Canonical Allele Identifier: PA2826648485
Gene: TXNRD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 432854
ClinVar RCV Id: RCV000628804 RCV000498644 RCV003159610
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269441.1:p.Met4Thr
CA410700165
NM_001282512.1:c.11T>C