Canonical Allele Identifier: PA916039278
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12559
ClinVar RCV Id: RCV000013387 RCV001800292 RCV003148621
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341642.1:p.Arg438His
CA122497
NM_001354713.2:c.1313G>A