Canonical Allele Identifier: PA2827269892
Gene: CAND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 161718
ClinVar RCV Id: RCV000149254
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001316605.1:p.Gly213Asp
CA174656
NM_001329676.2:c.638G>A