Canonical Allele Identifier: PA2825439980
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Val319Met
CA394315689
NM_001077183.3:c.955G>A