Canonical Allele Identifier: PA176047
Gene: ERBB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 163410
ClinVar RCV Id: RCV000150654

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276865.1:p.Gly761Val
CA176042
NM_001289936.2:c.2282G>T