Canonical Allele Identifier: PA109653
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 4826

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Thr721Met
CA253308
NM_000441.2:c.2162C>T