Canonical Allele Identifier: PA658801054
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 499395
ClinVar RCV Id: RCV000593909 RCV000804550
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Asp176Gly
CA2112638
NM_000784.4:c.527A>G