Allele Registry

Canonical Allele Identifier: PA645415107

Gene: SLC26A2 HGNC NCBI

ClinVar RCV:

RCV000324346

RCV000956326

RCV001271508

RCV001707611

ClinVar Variation:

284376

HGVS (amino-acid)	Matching Registered Transcripts
NP_000103.2:p.Asn696Ser	CA3505551 NM_000112.4:c.2087A>G