ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA645387218
Gene: SLC26A4
HGNC
NCBI
Linked Data
ClinVar Variation Id:
371034
ClinVar RCV Id:
RCV000411778
RCV000770857
RCV001850953
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000432.1:p.Thr94Ile
CA16041101
NM_000441.2:c.281C>T