Canonical Allele Identifier: PA2829974812
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467907

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Met649Val
CA034654
NM_021055.3:c.1945A>G