Canonical Allele Identifier: PA2826353908
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 2633292
ClinVar RCV Id: RCV003400020
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001239563.1:p.Gly344Arg
CA351888719
NM_001252634.2:c.1030G>C
CA351888720
NM_001252634.2:c.1030G>A