Allele Registry

Canonical Allele Identifier: PA102173

Gene: SLC26A3 HGNC NCBI

ClinVar RCV:

RCV000049417

ClinVar Variation:

56008

HGVS (amino-acid)	Matching Registered Transcripts
NP_000102.1:p.His220Pro	CA144113 NM_000111.3:c.659A>C