Allele Registry

Canonical Allele Identifier: PA645414967

Gene: SLC26A2 HGNC NCBI

ClinVar RCV:

RCV000398136

RCV000539759

RCV000987616

RCV001154133

RCV001154972

RCV001154973

RCV001154974

RCV001812767

ClinVar Variation:

281118

HGVS (amino-acid)	Matching Registered Transcripts
NP_000103.2:p.Asn77His	CA3505223 NM_000112.4:c.229A>C