Canonical Allele Identifier: PA915966127
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 691516
ClinVar RCV Id: RCV001004647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Ser657Asn
CA368843741
NM_000441.2:c.1970G>A