Canonical Allele Identifier: PA658722262
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 492916
ClinVar RCV Id: RCV000584605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001239563.1:p.Ser314Phe
CA351888908
NM_001252634.2:c.941C>T