Canonical Allele Identifier: PA2825572050
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467927

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Lys72Arg
CA394303587
NM_001114382.3:c.215A>G