Allele Registry

Canonical Allele Identifier: PA3057313668

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV004702950

ClinVar Variation:

3339208

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Phe335Ile	CA4432661 NM_000441.2:c.1003T>A