Canonical Allele Identifier: PA2825665020
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 993157
ClinVar RCV Id: RCV001284365

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121648.1:p.Leu341Pro
CA351888738
NM_001128176.3:c.1022T>C