Canonical Allele Identifier: PA2825436147
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535909

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Pro672Ala
CA394274478
NM_001077183.3:c.2014C>G