Canonical Allele Identifier: PA2828410883
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207711

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Glu366Lys
CA028150
NM_001370404.1:c.1096G>A