Allele Registry

Canonical Allele Identifier: PA645387229

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV000414878

RCV003330659

ClinVar Variation:

373979

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Leu100Pro	CA16043422 NM_000441.2:c.299T>C