Canonical Allele Identifier: PA345285
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 65999
ClinVar RCV Id: RCV000056246
ClinVar Variation Id: 631846

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Trp133Ter