Canonical Allele Identifier: PA2829979515
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2626434
ClinVar RCV Id: RCV003382414

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Asp1179Glu
CA394292130
NM_021055.3:c.3537C>A
CA394292131
NM_021055.3:c.3537C>G