Canonical Allele Identifier: PA645426140
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 291259
ClinVar RCV Id: RCV000368208 RCV001138169 RCV002436128
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Gly372Arg
CA2112807
NM_000784.4:c.1114G>A
CA350592083
NM_000784.4:c.1114G>C