Canonical Allele Identifier: PA916056502
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 488168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542168.1:p.Gly158Ala
CA386781600
NM_080601.3:c.473G>C