Allele Registry

Canonical Allele Identifier: PA2741817501

Gene: SLC26A4 HGNC NCBI

ClinVar Allele:

2742185

ClinVar RCV:

RCV003324364

RCV003475561

ClinVar Variation:

2577287

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Val196Asp	CA368848416 NM_000441.2:c.587T>A