Canonical Allele Identifier: PA2580117152
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2041909
ClinVar RCV Id: RCV002903337
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Glu359Ala
CA350591703
NM_000784.4:c.1076A>C