Canonical Allele Identifier: PA2573170208
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1394319
ClinVar RCV Id: RCV001900877

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Gly707Val
CA368845576
NM_000441.2:c.2120G>T