Canonical Allele Identifier: PA2825437491
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468013

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Val1095Ile
CA046764
NM_001077183.3:c.3283G>A