Canonical Allele Identifier: PA2825574099
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2869772
ClinVar RCV Id: RCV003626367

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ala673Ser
CA394274492
NM_001114382.3:c.2017G>T