Canonical Allele Identifier: PA2825437040
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2564721
ClinVar RCV Id: RCV003297153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Leu956Ser
CA394283775
NM_001077183.3:c.2867T>C