Canonical Allele Identifier: PA2580115183
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1962121
ClinVar RCV Id: RCV002725899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Lys715Arg
CA368845755
NM_000441.2:c.2144A>G