Canonical Allele Identifier: PA2825436047
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467907

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Met649Val
CA034654
NM_001077183.3:c.1945A>G