Canonical Allele Identifier: PA267617
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40521
ClinVar RCV Id: RCV000106324 RCV000526885
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Leu262Arg
CA267615
NM_002834.5:c.785T>G