Canonical Allele Identifier: PA132706
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 43540

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Ile713Met
CA132705
NM_000441.2:c.2139T>G