Canonical Allele Identifier: PA2827641794
Gene: TXNRD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 263784
ClinVar RCV Id: RCV000253691 RCV000470015 RCV000441585 RCV001528755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339229.1:p.Gly383Ser
CA10103786
NM_001352300.2:c.1147G>A