Canonical Allele Identifier: PA158608
Gene: ERBB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 134074
ClinVar RCV Id: RCV000120745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276865.1:p.Met30Val
CA158601
NM_001289936.2:c.88A>G