Canonical Allele Identifier: PA2828094768
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 265281

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Glu1517Lys
CA10588598
NM_001363528.2:c.4549G>A