Canonical Allele Identifier: PA645426113
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 288055
ClinVar RCV Id: RCV000282062 RCV003105851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.His362Arg
CA10605957
NM_000784.4:c.1085A>G