Canonical Allele Identifier: PA645424821
Gene: CCDC40 HGNC NCBI

Linked Data

ClinVar Variation Id: 407773

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060420.2:p.Asn396Ile
CA8813733
NM_017950.4:c.1187A>T