Canonical Allele Identifier: PA2827926335
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 429021
ClinVar RCV Id: RCV000579271

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341644.1:p.Leu310Val
CA351888740
NM_001354715.2:c.928C>G