Allele Registry

Canonical Allele Identifier: PA2741817548

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV003844436

ClinVar Variation:

2988253

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Trp482Arg	CA368841188 NM_000441.2:c.1444T>A CA368841189 NM_000441.2:c.1444T>C