Canonical Allele Identifier: PA2825572545
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406017

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Val225Met
CA056118
NM_001114382.3:c.673G>A