Canonical Allele Identifier: PA345166
Gene: CYP27A1 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Pro401Arg
CA345165
NM_000784.4:c.1202C>G