Canonical Allele Identifier: PA2573173642
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1482764
ClinVar RCV Id: RCV002025260
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Trp268Cys
CA350587342
NM_000784.4:c.804G>C
CA350587346
NM_000784.4:c.804G>T