Allele Registry

Canonical Allele Identifier: PA2499232495

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV001580202

ClinVar Variation:

1210160

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Phe335Val	CA368838305 NM_000441.2:c.1003T>G