Canonical Allele Identifier: PA2741817525
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2867731
ClinVar RCV Id: RCV003702918
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Val343Leu
CA368838428
NM_000441.2:c.1027G>T
CA368838432
NM_000441.2:c.1027G>C