Canonical Allele Identifier: PA916039256
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 12539
ClinVar RCV Id: RCV000013366 RCV000759364 RCV001281692
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341642.1:p.Thr337del
CA122458
NM_001354713.2:c.1010_1012del
CA71608607
NM_001354713.2:c.1009_1011del