Canonical Allele Identifier: PA109758
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 43495
ClinVar RCV Id: RCV000036427 RCV001171536 RCV002272039 RCV003473262 RCV004528181
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Val402Met
CA261400
NM_000441.2:c.1204G>A