Canonical Allele Identifier: PA2580115188
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2429150
ClinVar RCV Id: RCV003123389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Asp724Val
CA368845889
NM_000441.2:c.2171A>T