Canonical Allele Identifier: PA2825146262
Gene: THRB HGNC NCBI
ClinVar RCV:
RCV000508052
ClinVar Variation:
439308
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000452.2:p.Gly385Glu
CA351887119
NM_000461.5:c.1154G>A