Canonical Allele Identifier: PA2827642116
Gene: TXNRD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 263411
ClinVar RCV Id: RCV000247634 RCV000428455 RCV001521002
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339230.1:p.Ser269Arg
CA10103952
NM_001352301.2:c.805A>C
CA410686528
NM_001352301.2:c.807C>G
CA410686530
NM_001352301.2:c.807C>A