Canonical Allele Identifier: PA2828095027
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Lys1592Arg
CA16615040
NM_001363528.2:c.4775A>G