Canonical Allele Identifier: PA2828092595
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 959178

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Ile885Met
CA394279216
NM_001363528.2:c.2655C>G