Canonical Allele Identifier: PA2828530630
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 40535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361554.1:p.Asn307Thr
CA261607
NM_001374625.1:c.920A>C