Canonical Allele Identifier: PA2580115095
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1998024
ClinVar RCV Id: RCV002810155
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Phe346Leu
CA368838477
NM_000441.2:c.1036T>C
CA368838486
NM_000441.2:c.1038C>A
CA368838489
NM_000441.2:c.1038C>G