Canonical Allele Identifier: PA111647
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 993157
ClinVar RCV Id: RCV001284365
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000452.2:p.Leu341Pro
CA351888738
NM_000461.5:c.1022T>C