Canonical Allele Identifier: PA658817698
Gene: CCDC40 HGNC NCBI

Linked Data

ClinVar Variation Id: 525439
ClinVar RCV Id: RCV000629497 RCV001125859 RCV003420089
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060420.2:p.Arg493Ser
CA8813857
NM_017950.4:c.1479G>T
CA401326700
NM_017950.4:c.1479G>C