Canonical Allele Identifier: PA658826962
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 555073
ClinVar RCV Id: RCV000670819 RCV003228978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Ile491Thr
CA4432832
NM_000441.2:c.1472T>C