Canonical Allele Identifier: PA2828095635
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405970
ClinVar RCV Id: RCV000465811 RCV002348292
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Glu1735Asp
CA16615209
NM_001363528.2:c.5205G>T
CA394316180
NM_001363528.2:c.5205G>C