Canonical Allele Identifier: PA357178
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 224093

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Ala392Thr
CA357176
NM_002834.5:c.1174G>A