Canonical Allele Identifier: PA645452556
Gene: TRH HGNC NCBI

Linked Data

ClinVar Variation Id: 260114
ClinVar RCV Id: RCV000246814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009048.1:p.Leu8Val
CA2609908
NM_007117.5:c.22C>G