Canonical Allele Identifier: PA916015552
Gene: CCDC65 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273886.1:p.Ile40Met
CA6543274
NM_001286957.2:c.120A>G