Allele Registry

Canonical Allele Identifier: PA102106

Gene: SLC26A3 HGNC NCBI

ClinVar RCV:

RCV000049381

ClinVar Variation:

55972

HGVS (amino-acid)	Matching Registered Transcripts
NP_000102.1:p.Asp468Val	CA144055 NM_000111.3:c.1403A>T