Canonical Allele Identifier: PA2827006715
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Glu356Gln
CA028805
NM_001318829.2:c.1066G>C