Canonical Allele Identifier: PA122488
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12553
ClinVar RCV Id: RCV000013380 RCV000622278 RCV000760097
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121649.1:p.Arg320His
CA122487
NM_001128177.2:c.959G>A