Canonical Allele Identifier: PA2580493429
Gene: CCDC97 HGNC NCBI
ClinVar RCV:
RCV004236026
ClinVar Variation:
2399285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443080.1:p.Glu229Lys
CA9459699
NM_052848.3:c.685G>A