Canonical Allele Identifier: PA2825576594
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 641928
ClinVar RCV Id: RCV000795284

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Asp1455Val
CA394302256
NM_001114382.3:c.4364A>T