Canonical Allele Identifier: PA2827318337
Gene: CCDC40 HGNC NCBI

Linked Data

ClinVar Variation Id: 525439
ClinVar RCV Id: RCV000629497 RCV001125859 RCV003420089
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317437.1:p.Arg493Ser
CA8813857
NM_001330508.2:c.1479G>T
CA401326700
NM_001330508.2:c.1479G>C