Canonical Allele Identifier: PA180741
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13332

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Ser502Thr
CA180739
NM_002834.5:c.1504T>A