Canonical Allele Identifier: PA2827925490
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 619919
ClinVar RCV Id: RCV000760091

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341637.1:p.Leu456Ser
CA351886479
NM_001354708.2:c.1367T>C