Canonical Allele Identifier: PA2828554287
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 2442325
ClinVar RCV Id: RCV003149098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361753.1:p.Pro453Asn
CA2580069619
NM_001374824.1:c.1357_1358delinsAA