Canonical Allele Identifier: PA2827008748
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 184243

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Glu1087Lys
CA019256
NM_001318829.2:c.3259G>A