Canonical Allele Identifier: PA345182
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 65851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Gly472Ala
CA345181
NM_000784.4:c.1415G>C