Canonical Allele Identifier: PA220139
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40558
ClinVar RCV Id: RCV000033545 RCV000210040 RCV000515165 RCV000824750 RCV001028095 RCV001374913 RCV002390131 RCV004532494
ClinVar Variation Id: 40559
ClinVar RCV Id: RCV000033546 RCV000077852 RCV000157015 RCV000660241 RCV000618529 RCV000762886 RCV000824749 RCV001813261 RCV003147310 RCV003147311 RCV004532495
ClinVar Variation Id: 571101
ClinVar RCV Id: RCV000692146
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Gly503Arg
CA220137
NM_002834.5:c.1507G>A
CA273459
NM_002834.5:c.1507G>C
CA891844000
NM_002834.5:c.1506_1507delinsCC