Canonical Allele Identifier: PA658801067
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 500465
ClinVar RCV Id: RCV000595187 RCV000665470
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Glu392Ala
CA350592713
NM_000784.4:c.1175A>C