Canonical Allele Identifier: PA2573063727
Gene: CYP27B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1343091
ClinVar RCV Id: RCV001843693

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000776.1:p.Cys411Tyr
CA385501225
NM_000785.4:c.1232G>A