Canonical Allele Identifier: PA2828089656
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535934

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Arg25Lys
CA056318
NM_001363528.2:c.74G>A