Canonical Allele Identifier: PA2825577245
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Lys1635Arg
CA16615040
NM_001114382.3:c.4904A>G