Canonical Allele Identifier: PA645424607
Gene: CCDC40 HGNC NCBI

Linked Data

ClinVar Variation Id: 260974

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060420.2:p.Thr157Ile
CA8813446
NM_017950.4:c.470C>T