ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA132657
Gene: SLC26A4
HGNC
NCBI
Linked Data
ClinVar Variation Id:
43492
ClinVar RCV Id:
RCV000036423
RCV000756644
RCV000987940
RCV001004634
RCV003990962
RCV004541095
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000432.1:p.Phe354Ser
CA132656
NM_000441.2:c.1061T>C