Canonical Allele Identifier: PA2499232496
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1214607
ClinVar RCV Id: RCV001583697 RCV001832811
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Met349Ile
CA4432667
NM_000441.2:c.1047G>A
CA368838529
NM_000441.2:c.1047G>C
CA368838531
NM_000441.2:c.1047G>T