Canonical Allele Identifier: PA2828920768
Gene: ERBB2 HGNC NCBI

Linked Data

ClinVar Variation Id: 939578
ClinVar RCV Id: RCV001209000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369711.1:p.Tyr273His
CA399281753
NM_001382782.1:c.817T>C