Canonical Allele Identifier: PA297087
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 181499
ClinVar RCV Id: RCV000159051 RCV001261017 RCV001526955 RCV002408715
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Phe285Tyr
CA297085
NM_002834.5:c.854T>A