Canonical Allele Identifier: PA109625
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 43498
ClinVar RCV Id: RCV000036430 RCV000268093 RCV000576483 RCV000515696 RCV000824770 RCV001291347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Thr410Met
CA261403
NM_000441.2:c.1229C>T