Canonical Allele Identifier: PA2825437920
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 951136

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Arg1224Leu
CA394293592
NM_001077183.3:c.3671G>T