Canonical Allele Identifier: PA2828411921
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237974
ClinVar RCV Id: RCV000231071 RCV000576038 RCV001080839
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Gly661Ser
CA035412
NM_001370404.1:c.1981G>A