Canonical Allele Identifier: PA2827364047
Gene: CCDC97 HGNC NCBI

Linked Data

ClinVar Variation Id: 2399285
ClinVar RCV Id: RCV004236026
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001333029.1:p.Glu164Lys
CA9459699
NM_001346100.2:c.490G>A