Canonical Allele Identifier: PA2825438107
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49282

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ser1274Arg
CA019836
NM_001077183.3:c.3822C>A
CA394299190
NM_001077183.3:c.3820A>C
CA394299211
NM_001077183.3:c.3822C>G