Canonical Allele Identifier: PA645425120
Gene: CCDC40 HGNC NCBI

Linked Data

ClinVar Variation Id: 414637
ClinVar RCV Id: RCV000463546 RCV001421091
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060420.2:p.Ile933Ser
CA8814346
NM_017950.4:c.2798T>G