Canonical Allele Identifier: PA109208
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 504511
ClinVar RCV Id: RCV000603987 RCV001868006 RCV003471971
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Ala411Pro
CA368839274
NM_000441.2:c.1231G>C