Canonical Allele Identifier: PA2826327056
Gene: CCDC40 HGNC NCBI

Linked Data

ClinVar Variation Id: 407773
ClinVar RCV Id: RCV000459225 RCV001122109 RCV003418174
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230271.1:p.Asn396Ile
CA8813733
NM_001243342.2:c.1187A>T