Allele Registry

Canonical Allele Identifier: PA645415108

Gene: SLC26A2 HGNC NCBI

ClinVar Allele:

302198

ClinVar RCV:

RCV000281557

RCV000330490

RCV000336484

RCV000372485

RCV000376030

RCV001439481

ClinVar Variation:

352031

HGVS (amino-acid)	Matching Registered Transcripts
NP_000103.2:p.Tyr710Cys	CA3505558 NM_000112.4:c.2129A>G