Allele Registry

Canonical Allele Identifier: PA102335

Gene: SLC26A2 HGNC NCBI

ClinVar RCV:

RCV000023570

RCV000055761

RCV000169017

RCV003234891

ClinVar Variation:

4094

HGVS (amino-acid)	Matching Registered Transcripts
NP_000103.2:p.Gly678Val	CA259844 NM_000112.4:c.2033G>T