Canonical Allele Identifier: PA2825437003
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 318323

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Lys945Arg
CA10648020
NM_001077183.3:c.2834A>G