Canonical Allele Identifier: PA915965270
Gene: CYP27B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 722611
ClinVar RCV Id: RCV000896271 RCV003910674
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000776.1:p.Ala129Thr
CA6658482
NM_000785.4:c.385G>A