Canonical Allele Identifier: PA645387218
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 371034
ClinVar RCV Id: RCV000411778 RCV000770857 RCV001850953
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Thr94Ile
CA16041101
NM_000441.2:c.281C>T