Canonical Allele Identifier: PA261609
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002825.3:p.Asn308Thr
CA261607
NM_002834.5:c.923A>C