Canonical Allele Identifier: PA2828091753
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467907

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Met649Val
CA034654
NM_001363528.2:c.1945A>G