Allele Registry

Canonical Allele Identifier: PA2573170201

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV002020992

ClinVar Variation:

1515298

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Leu676Pro	CA368843849 NM_000441.2:c.2027T>C