Canonical Allele Identifier: PA2825437377
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 141482

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ala1064Val
CA018885
NM_001077183.3:c.3191C>T