Canonical Allele Identifier: PA2827007006
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64996

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Arg456Gln
CA015034
NM_001318829.2:c.1367G>A