Canonical Allele Identifier: PA110645
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 4258
ClinVar RCV Id: RCV000004480 RCV001650828 RCV003415650
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Arg474Gln
CA340214
NM_000784.4:c.1421G>A