Canonical Allele Identifier: PA645463056
Gene: TSHR HGNC NCBI

Linked Data

ClinVar Variation Id: 314690

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000360.2:p.Ser53Arg
CA10646433
NM_000369.2:c.157A>C
CA390770753
NM_000369.2:c.159T>A
CA390770754
NM_000369.2:c.159T>G