Canonical Allele Identifier: PA2741817541
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2735069
ClinVar RCV Id: RCV003555360 RCV004527460
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Gly439Arg
CA4432774
NM_000441.2:c.1315G>A
CA368840374
NM_000441.2:c.1315G>C