Canonical Allele Identifier: PA658668687
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 446462
ClinVar RCV Id: RCV000515647
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Phe692Leu
CA368844476
NM_000441.2:c.2074T>C
CA368844488
NM_000441.2:c.2076T>A
CA368844490
NM_000441.2:c.2076T>G