Allele Registry

Canonical Allele Identifier: PA2499259713

Gene: DCT HGNC NCBI

ClinVar RCV:

RCV001678579

ClinVar Variation:

1268230

HGVS (amino-acid)	Matching Registered Transcripts
NP_001913.2:p.Gly59Val	CA388384727 NM_001922.5:c.176G>T