Canonical Allele Identifier: PA109379
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 4825
ClinVar RCV Id: RCV000005094 RCV000005095 RCV000036477 RCV000480319 RCV002476929 RCV004528078
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.His723Arg
CA253307
NM_000441.2:c.2168A>G