Canonical Allele Identifier: PA2825435896
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 318315

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ile606Val
CA033640
NM_001077183.3:c.1816A>G