Canonical Allele Identifier: PA2827926183
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12542
ClinVar RCV Id: RCV000013369 RCV000760096
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341643.1:p.Ala286Thr
CA122467
NM_001354714.2:c.856G>A