Canonical Allele Identifier: PA2827926397
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 619919
ClinVar RCV Id: RCV000760091

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341644.1:p.Leu425Ser
CA351886479
NM_001354715.2:c.1274T>C