Canonical Allele Identifier: PA2825434359
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Val109Met
CA045030
NM_001077183.3:c.325G>A