Allele Registry

Canonical Allele Identifier: PA2828130515

Gene: VDR HGNC NCBI

ClinVar Variation Id: 1038600

ClinVar RCV Id: RCV001341929

HGVS (amino-acid)	Matching Registered Transcripts
NP_001351014.1:p.Ala388Asp	CA384514186 NM_001364085.2:c.1163C>A