Canonical Allele Identifier: PA2827925688
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 801289
ClinVar RCV Id: RCV000986045
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341639.1:p.Met310Leu
CA351888941
NM_001354710.2:c.928A>T
CA351888943
NM_001354710.2:c.928A>C