Canonical Allele Identifier: PA174477
Gene: ERBB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 161622
ClinVar RCV Id: RCV000149158
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276865.1:p.Gln887His
CA174472
NM_001289936.2:c.2661G>C
CA399305639
NM_001289936.2:c.2661G>T