Canonical Allele Identifier: PA658722259
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 492915
ClinVar RCV Id: RCV000583370 RCV001800808
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001239563.1:p.Met313Thr
CA351888916
NM_001252634.2:c.938T>C