Canonical Allele Identifier: PA2825664994
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 801289
ClinVar RCV Id: RCV000986045
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121648.1:p.Met310Leu
CA351888941
NM_001128176.3:c.928A>T
CA351888943
NM_001128176.3:c.928A>C