Canonical Allele Identifier: PA1139745452
Gene: ERBB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 939578
ClinVar RCV Id: RCV001209000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369716.1:p.Tyr328His
CA399281753
NM_001382787.1:c.982T>C