Canonical Allele Identifier: PA158695
Gene: ERBB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 134086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001005862.1:p.Arg1200Leu
CA158691
NM_001005862.3:c.3599G>T