Canonical Allele Identifier: PA2825575836
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2626434
ClinVar RCV Id: RCV003382414

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Asp1222Glu
CA394292130
NM_001114382.3:c.3666C>A
CA394292131
NM_001114382.3:c.3666C>G