Canonical Allele Identifier: PA2827926398
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 1809577
ClinVar RCV Id: RCV002481152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341644.1:p.Glu426Asp
CA351886467
NM_001354715.2:c.1278A>T
CA351886468
NM_001354715.2:c.1278A>C