Allele Registry

Canonical Allele Identifier: PA345168

Gene: CYP27A1 HGNC NCBI

ClinVar Allele:

76745

ClinVar RCV:

RCV000056077

ClinVar Variation:

65837

HGVS (amino-acid)	Matching Registered Transcripts
NP_000775.1:p.Asn403Lys	CA345167 NM_000784.4:c.1209C>G CA350593104 NM_000784.4:c.1209C>A