Canonical Allele Identifier: PA916056426
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Asp61His
CA282070
NM_080601.3:c.181G>C