Canonical Allele Identifier: PA2827313109
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13328

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Tyr279Cys
CA220149
NM_001330437.2:c.836A>G