Canonical Allele Identifier: PA2580115177
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2436006
ClinVar RCV Id: RCV003136756

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Ile700Val
CA368845457
NM_000441.2:c.2098A>G