Canonical Allele Identifier: PA2827312836
Gene: PTPN11 HGNC NCBI

Linked Data

ClinVar Variation Id: 13337

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317366.1:p.Glu76Val
CA123041
NM_001330437.2:c.227A>T