Canonical Allele Identifier: PA2826326989
Gene: CCDC40 HGNC NCBI

Linked Data

ClinVar Variation Id: 260979
ClinVar RCV Id: RCV000244307 RCV000399959 RCV001094519 RCV001283738 RCV001544955
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230271.1:p.Asp284His
CA8813582
NM_001243342.2:c.850G>C