Allele Registry

Canonical Allele Identifier: PA645387350

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV000409144

RCV001069495

ClinVar Variation:

371146

862716

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Ser391Arg	CA16041107 NM_000441.2:c.1173C>A CA368839153 NM_000441.2:c.1171A>C CA368839158 NM_000441.2:c.1173C>G