Canonical Allele Identifier: PA340224
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 4267

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Arg479Gly
CA340223
NM_000784.4:c.1435C>G