Canonical Allele Identifier: PA2827926038
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 492921
ClinVar RCV Id: RCV000584262 RCV002469212 RCV003389056 RCV003392424
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341641.1:p.Arg438Cys
CA71604941
NM_001354712.2:c.1312C>T