Canonical Allele Identifier: PA109322
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 4839
ClinVar RCV Id: RCV000005111 RCV000036509 RCV000169251 RCV000656195 RCV001040420 RCV002496264 RCV004528081
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Glu29Gln
CA253315
NM_000441.2:c.85G>C