Canonical Allele Identifier: PA2828095434
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406083

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Glu1691Lys
CA16615048
NM_001363528.2:c.5071G>A