Canonical Allele Identifier: PA2828925932
Gene: ERBB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 44991
ClinVar Variation Id: 376036
ClinVar RCV Id: RCV000439788

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369721.1:p.Val765Leu
CA135387
NM_001382792.1:c.2293G>T
CA16602503
NM_001382792.1:c.2293G>C