Canonical Allele Identifier: PA2827925383
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_001341637.1:p.Ala234Val
CA351891391
NM_001354708.2:c.701C>T