Canonical Allele Identifier: PA2829975680
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 12398

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Leu717Arg
CA016832
NM_021055.3:c.2150T>G