Canonical Allele Identifier: PA2825576357
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Arg1386Gly
CA276753368
NM_001114382.3:c.4156C>G