Canonical Allele Identifier: PA2573062768
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1309671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Thr745Met
CA4433084
NM_000441.2:c.2234C>T