Canonical Allele Identifier: PA2825438247
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65353

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Pro1314Leu
CA020000
NM_001077183.3:c.3941C>T