Canonical Allele Identifier: PA132659
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 43499
ClinVar RCV Id: RCV000036431 RCV000670464 RCV001785457 RCV002490496 RCV003137559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Val412Ile
CA132658
NM_000441.2:c.1234G>A