Canonical Allele Identifier: PA2573170207
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1297074

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Leu703Val
CA368845496
NM_000441.2:c.2107C>G