Canonical Allele Identifier: PA916028161
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 265307

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Thr511Lys
CA10588540
NM_001330437.2:c.1532C>A