Canonical Allele Identifier: PA645425189
Gene: CCDC40 HGNC NCBI

Linked Data

ClinVar Variation Id: 260965
ClinVar RCV Id: RCV000247767 RCV000400322 RCV001094548 RCV001549870
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060420.2:p.Arg967His
CA8814543
NM_017950.4:c.2900G>A