Canonical Allele Identifier: PA2827018945
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 64875

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ala1128Val
CA019204
NM_001318832.2:c.3383C>T