Canonical Allele Identifier: PA2827313086
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Leu262Arg
CA267615
NM_001330437.2:c.785T>G