Canonical Allele Identifier: PA2825437344
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405953

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Pro1054Leu
CA045588
NM_001077183.3:c.3161C>T