Canonical Allele Identifier: PA658801051
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 502427
ClinVar RCV Id: RCV000595155 RCV001423428
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Ala172Val
CA2112632
NM_000784.4:c.515C>T