Canonical Allele Identifier: PA261586
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40506
ClinVar RCV Id: RCV000033483 RCV000157021 RCV000212893 RCV001261998 RCV001813247
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Asp106Ala
CA261584
NM_002834.5:c.317A>C