Canonical Allele Identifier: PA2827926394
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 2442325
ClinVar RCV Id: RCV003149098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341644.1:p.Pro422Asn
CA2580069619
NM_001354715.2:c.1264_1265delinsAA