Canonical Allele Identifier: PA2825437546
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Pro1112Leu
CA046958
NM_001077183.3:c.3335C>T