Canonical Allele Identifier: PA2828094419
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Glu1424Gly
CA051259
NM_001363528.2:c.4271A>G