Canonical Allele Identifier: PA2825439084
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468116

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ala1550Gly
CA394308217
NM_001077183.3:c.4649C>G