Canonical Allele Identifier: PA645426103
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 281718
ClinVar RCV Id: RCV000290127 RCV001341973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Val307Leu
CA2112758
NM_000784.4:c.919G>T
CA350588428
NM_000784.4:c.919G>C