Canonical Allele Identifier: PA345200
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 65868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Gly145Arg
CA345199
NM_000784.4:c.433G>A
CA350584123
NM_000784.4:c.433G>C