Canonical Allele Identifier: PA2828928997
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_001369727.1:p.Val777Leu
CA135387
NM_001382798.1:c.2329G>T
CA16602503
NM_001382798.1:c.2329G>C