Canonical Allele Identifier: PA261548
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40551
ClinVar RCV Id: RCV000033537 RCV000037617 RCV001378165 RCV002490446 RCV001730478 RCV002390130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Pro491His
CA261546
NM_002834.5:c.1472C>A