Canonical Allele Identifier: PA2573170182
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1297072
ClinVar RCV Id: RCV002051741

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Phe572Leu
CA368842825
NM_000441.2:c.1714T>C
CA368842831
NM_000441.2:c.1716T>A
CA368842832
NM_000441.2:c.1716T>G