Canonical Allele Identifier: PA261539
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40546
ClinVar RCV Id: RCV000033529 RCV000037612 RCV001060541 RCV001729356
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Ala461Ser
CA261537
NM_002834.5:c.1381G>T