Canonical Allele Identifier: PA2825573008
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 429535

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ile365Val
CA028137
NM_001114382.3:c.1093A>G