Allele Registry

Canonical Allele Identifier: PA102271

Gene: SLC26A3 HGNC NCBI

ClinVar Allele:

70619

ClinVar RCV:

RCV000049389

ClinVar Variation:

55980

HGVS (amino-acid)	Matching Registered Transcripts
NP_000102.1:p.Tyr520Cys	CA144065 NM_000111.3:c.1559A>G