Allele Registry

Canonical Allele Identifier: PA263271

Gene: SLC26A2 HGNC NCBI

ClinVar RCV:

RCV000049434

ClinVar Variation:

56025

HGVS (amino-acid)	Matching Registered Transcripts
NP_000103.2:p.Gly166Arg	CA263269 NM_000112.4:c.496G>A CA361705111 NM_000112.4:c.496G>C