Canonical Allele Identifier: PA2827019718
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2506402
ClinVar RCV Id: RCV003234985

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Gly1352Asp
CA394300149
NM_001318832.2:c.4055G>A