Canonical Allele Identifier: PA2580115097
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2104163
ClinVar RCV Id: RCV003031244
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Ala351Gly
CA4432668
NM_000441.2:c.1052C>G