Canonical Allele Identifier: PA282072
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Asp61His
CA282070
NM_002834.5:c.181G>C