Canonical Allele Identifier: PA110684
Gene: CYP27B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1658
ClinVar RCV Id: RCV000001725 RCV001195100
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000776.1:p.Arg107His
CA115124
NM_000785.4:c.320G>A