Canonical Allele Identifier: PA2573173878
Gene: CYP27B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1352793
ClinVar RCV Id: RCV002039957

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000776.1:p.Ala329Val
CA385504041
NM_000785.4:c.986C>T