Canonical Allele Identifier: PA2827925769
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 439310

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341639.1:p.Pro453Ser
CA351886499
NM_001354710.2:c.1357C>T