Canonical Allele Identifier: PA2825438025
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Glu1254Val
CA019757
NM_001077183.3:c.3761A>T