Canonical Allele Identifier: PA2827925407
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 492916
ClinVar RCV Id: RCV000584605

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341637.1:p.Ser314Phe
CA351888908
NM_001354708.2:c.941C>T