Canonical Allele Identifier: PA2499232498
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1028755
ClinVar RCV Id: RCV001329891 RCV002546359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Val412Phe
CA368839280
NM_000441.2:c.1234G>T