Allele Registry

Canonical Allele Identifier: PA102191

Gene: SLC26A3 HGNC NCBI

ClinVar RCV:

RCV000049384

ClinVar Variation:

55975

HGVS (amino-acid)	Matching Registered Transcripts
NP_000102.1:p.Leu496Arg	CA144059 NM_000111.3:c.1487T>G