Canonical Allele Identifier: PA1139743851
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 993241
ClinVar RCV Id: RCV001284715

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361755.1:p.Phe459Leu
CA351886455
NM_001374826.1:c.1377C>G
CA351886456
NM_001374826.1:c.1377C>A
CA351886460
NM_001374826.1:c.1375T>C