Canonical Allele Identifier: PA658826992
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 557592
ClinVar RCV Id: RCV000673751

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Glu704Lys
CA368845507
NM_000441.2:c.2110G>A