Canonical Allele Identifier: PA118196
Gene: TSHR HGNC NCBI
ClinVar RCV:
RCV000006800
ClinVar Variation:
6431
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Asp619Gly
CA118194
NM_000369.2:c.1856A>G