Allele Registry

Canonical Allele Identifier: PA102224

Gene: SLC26A3 HGNC NCBI

ClinVar RCV:

RCV000049408

RCV003556126

ClinVar Variation:

55999

HGVS (amino-acid)	Matching Registered Transcripts
NP_000102.1:p.Pro131Arg	CA144097 NM_000111.3:c.392C>G