Canonical Allele Identifier: PA2580493438
Gene: CCDC97 HGNC NCBI

Linked Data

ClinVar Variation Id: 2292883
ClinVar RCV Id: RCV004146446
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443080.1:p.Arg292Cys
CA9459783
NM_052848.3:c.874C>T