Canonical Allele Identifier: PA2827318264
Gene: CCDC40 HGNC NCBI

Linked Data

ClinVar Variation Id: 260949

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317437.1:p.Ile407Thr
CA8813739
NM_001330508.2:c.1220T>C