Allele Registry

Canonical Allele Identifier: PA2573062756

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV001766991

RCV003323925

ClinVar Variation:

1306038

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Val422Gly	CA368840241 NM_000441.2:c.1265T>G