Canonical Allele Identifier: PA645387412
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 370080
ClinVar RCV Id: RCV000411469 RCV001216381 RCV001291348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Gln413Arg
CA4432728
NM_000441.2:c.1238A>G