Canonical Allele Identifier: PA345198
Gene: CYP27A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 65867
ClinVar RCV Id: RCV000056112 RCV001268892 RCV003894909
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000775.1:p.Arg137Trp
CA345197
NM_000784.4:c.409C>T