Canonical Allele Identifier: PA2827926156
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 619920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341643.1:p.Ala203Val
CA351891391
NM_001354714.2:c.608C>T