Canonical Allele Identifier: PA2580115190
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1801126
ClinVar RCV Id: RCV002462723

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Gln732Lys
CA368845995
NM_000441.2:c.2194C>A