Canonical Allele Identifier: PA2828091892
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237977

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Leu681Gln
CA10583301
NM_001363528.2:c.2042T>A