Canonical Allele Identifier: PA916039227
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 619920
ClinVar RCV Id: RCV000760092 RCV003392578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341642.1:p.Ala234Val
CA351891391
NM_001354713.2:c.701C>T