Canonical Allele Identifier: PA2827364054
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_001333029.1:p.Arg227Cys
CA9459783
NM_001346100.2:c.679C>T