Canonical Allele Identifier: PA916022783
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65349

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Glu77Lys
CA019111
NM_001318827.2:c.229G>A