Canonical Allele Identifier: PA261564
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40493

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Gly60Ala
CA261562
NM_002834.5:c.179G>C