Canonical Allele Identifier: PA109225
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 43497
ClinVar RCV Id: RCV000036429 RCV001291346 RCV001814025 RCV002513381 RCV003473263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Arg409Pro
CA261402
NM_000441.2:c.1226G>C