Canonical Allele Identifier: PA2741816310
Gene: TSHR HGNC NCBI
ClinVar RCV:
RCV004531768
ClinVar Variation:
2634929
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Ala553Ser
CA7294506
NM_000369.2:c.1657G>T