Allele Registry

Canonical Allele Identifier: PA2573162891

Gene: SLC26A2 HGNC NCBI

ClinVar RCV:

RCV002238704

ClinVar Variation:

1683432

HGVS (amino-acid)	Matching Registered Transcripts
NP_000103.2:p.Val341dup	CA917608031 NM_000112.4:c.1020_1022dup