Allele Registry

Canonical Allele Identifier: PA915979845

Gene: TSHR HGNC NCBI

ClinVar RCV:

RCV000308671

RCV000400375

RCV000489665

RCV003153557

RCV003335304

ClinVar Variation:

314693

HGVS (amino-acid)	Matching Registered Transcripts
NP_001136098.1:p.Gly132Arg	CA7294130 NM_001142626.3:c.394G>C