Canonical Allele Identifier: PA2580117594
Gene: CYP27B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1936106
ClinVar RCV Id: RCV002657933

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000776.1:p.Thr406Met
CA6658172
NM_000785.4:c.1217C>T