Canonical Allele Identifier: PA122455
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12536
ClinVar RCV Id: RCV000013363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121649.1:p.Gln340His
CA122454
NM_001128177.2:c.1020G>C
CA351888742
NM_001128177.2:c.1020G>T