Canonical Allele Identifier: PA2827364055
Gene: CCDC97 HGNC NCBI

Linked Data

ClinVar Variation Id: 2371401
ClinVar RCV Id: RCV004212244
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333029.1:p.Tyr238Cys
CA9459791
NM_001346100.2:c.713A>G