Canonical Allele Identifier: PA264562
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65095
ClinVar RCV Id: RCV000055306 RCV003512006
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Leu1548Pro
CA020803
NM_000548.5:c.4643T>C