Canonical Allele Identifier: PA158606
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_001005862.1:p.Met15Val
CA158601
NM_001005862.3:c.43A>G