Canonical Allele Identifier: PA645424856
Gene: CCDC40 HGNC NCBI

Linked Data

ClinVar Variation Id: 414641
ClinVar RCV Id: RCV001124881 RCV000469694
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060420.2:p.Ala458Thr
CA8813803
NM_017950.4:c.1372G>A