Canonical Allele Identifier: PA2499232510
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1065206
ClinVar RCV Id: RCV001375682

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Thr721Lys
CA368845842
NM_000441.2:c.2162C>A