Canonical Allele Identifier: PA2741817501
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2577287
ClinVar RCV Id: RCV003324364 RCV003475561
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Val196Asp
CA368848416
NM_000441.2:c.587T>A