Canonical Allele Identifier: PA645387255
Gene: SLC26A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 423822
ClinVar RCV Id: RCV000480978 RCV001785632 RCV001785633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000432.1:p.Ala179Thr
CA4432504
NM_000441.2:c.535G>A