Canonical Allele Identifier: PA274087
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 188889
ClinVar RCV Id: RCV000169245 RCV000515737 RCV001048975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Val659Leu
CA274086
NM_000441.2:c.1975G>C
CA368843751
NM_000441.2:c.1975G>T