Canonical Allele Identifier: PA110848
Gene: CYP27B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1668
ClinVar RCV Id: RCV000001735 RCV001234461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000776.1:p.Thr409Ile
CA115132
NM_000785.4:c.1226C>T