Canonical Allele Identifier: PA2741817569
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2682260

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Asp697Gly
CA368845412
NM_000441.2:c.2090A>G