Canonical Allele Identifier: PA261551
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40555
ClinVar RCV Id: RCV000033541 RCV000037618 RCV000466382 RCV001800333 RCV002260947 RCV004018716
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Arg501Lys
CA261549
NM_002834.5:c.1502G>A