Canonical Allele Identifier: PA203236
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 65831
ClinVar RCV Id: RCV000056071 RCV000179342 RCV001698579 RCV002345362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Pro384Leu
CA203235
NM_000784.4:c.1151C>T