Canonical Allele Identifier: PA2825434094
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2706786
ClinVar RCV Id: RCV003512954

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Arg25Met
CA394301232
NM_001077183.3:c.74G>T