Canonical Allele Identifier: PA122462
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12539

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001239563.1:p.Thr337del
CA122458
NM_001252634.2:c.1010_1012del
CA71608607
NM_001252634.2:c.1009_1011del