Canonical Allele Identifier: PA2827000243
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207700

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Lys107Arg
CA050850
NM_001318827.2:c.320A>G