ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2827641567
Gene: TXNRD2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
654863
ClinVar RCV Id:
RCV000810915
RCV002453831
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001339229.1:p.Tyr112Cys
CA410693741
NM_001352300.2:c.335A>G