Canonical Allele Identifier: PA2825146291
Gene: THRB HGNC NCBI

Linked Data

ClinVar Variation Id: 2442325
ClinVar RCV Id: RCV003149098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000452.2:p.Pro453Asn
CA2580069619
NM_000461.5:c.1357_1358delinsAA