Canonical Allele Identifier: PA2827318313
Gene: CCDC40 HGNC NCBI

Linked Data

ClinVar Variation Id: 414641

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317437.1:p.Ala458Thr
CA8813803
NM_001330508.2:c.1372G>A