Canonical Allele Identifier: PA2827926000
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 429021
ClinVar RCV Id: RCV000579271
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341641.1:p.Leu341Val
CA351888740
NM_001354712.2:c.1021C>G