Allele Registry

Canonical Allele Identifier: PA2827926190

Gene: THRB HGNC NCBI

ClinVar RCV:

RCV000449629

ClinVar Variation:

397581

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341643.1:p.Glu295Gly	CA16609441 NM_001354714.2:c.884A>G