Canonical Allele Identifier: PA2827312760
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Asp61His
CA282070
NM_001330437.2:c.181G>C