Canonical Allele Identifier: PA2573173707
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1376283
ClinVar RCV Id: RCV001885808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Ala388Thr
CA350592586
NM_000784.4:c.1162G>A