Canonical Allele Identifier: PA2573062755
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1331128
ClinVar RCV Id: RCV001806473

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Phe346Ile
CA368838475
NM_000441.2:c.1036T>A