Canonical Allele Identifier: PA2825573711
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ala580Gly
CA033236
NM_001114382.3:c.1739C>G