Canonical Allele Identifier: PA2825435155
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405972

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Leu372Pro
CA16614653
NM_001077183.3:c.1115T>C