Canonical Allele Identifier: PA2741817570
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2637453
ClinVar RCV Id: RCV003404751

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Asp697Glu
CA368845416
NM_000441.2:c.2091T>A
CA368845418
NM_000441.2:c.2091T>G