Canonical Allele Identifier: PA261599
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40523
ClinVar RCV Id: RCV000033502 RCV000037660 RCV000703823 RCV001729355 RCV003147308 RCV003147309 RCV004545735
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Gly268Cys
CA261597
NM_002834.5:c.802G>T