Canonical Allele Identifier: PA2828414591
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Glu1446Gly
CA051259
NM_001370404.1:c.4337A>G