Allele Registry

Canonical Allele Identifier: PA261431

Gene: SLC26A4 HGNC NCBI

ClinVar RCV:

RCV000036489

RCV000797012

RCV001273161

RCV001329893

RCV003114215

ClinVar Variation:

43553

HGVS (amino-acid)	Matching Registered Transcripts
NP_000432.1:p.Met1Thr