Canonical Allele Identifier: PA2826327048
Gene: CCDC40 HGNC NCBI

Linked Data

ClinVar Variation Id: 241231
ClinVar RCV Id: RCV000228173
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230271.1:p.Ala380Thr
CA8813695
NM_001243342.2:c.1138G>A