Canonical Allele Identifier: PA2825574091
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1399324

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Gly671Ser
CA394274467
NM_001114382.3:c.2011G>A