Allele Registry

Canonical Allele Identifier: PA2580341043

Gene: TRH HGNC NCBI

ClinVar RCV:

RCV003142767

ClinVar Variation:

2437264

HGVS (amino-acid)	Matching Registered Transcripts
NP_009048.1:p.Arg226Trp	CA2610091 NM_007117.5:c.676C>T