Canonical Allele Identifier: PA2829980105
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135384
ClinVar Variation Id: 2837265
ClinVar RCV Id: RCV003628312

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Glu1278Asp
CA019763
NM_021055.3:c.3834G>C
CA394297480
NM_021055.3:c.3834G>T