Canonical Allele Identifier: PA2827925634
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 1809577
ClinVar RCV Id: RCV002481152

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341638.1:p.Glu457Asp
CA351886467
NM_001354709.2:c.1371A>T
CA351886468
NM_001354709.2:c.1371A>C