Canonical Allele Identifier: PA2826770568
Gene: ERBB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 939578
ClinVar RCV Id: RCV001209000

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276866.1:p.Tyr303His
CA399281753
NM_001289937.2:c.907T>C