Allele Registry

Canonical Allele Identifier: PA149719

Gene: SLC26A5 HGNC NCBI

ClinVar RCV:

RCV000083266

ClinVar Variation:

97020

HGVS (amino-acid)	Matching Registered Transcripts
NP_996766.1:p.Arg130Ser	CA149718 NM_206883.3:c.390A>C CA368767410 NM_206883.3:c.390A>T