Canonical Allele Identifier: PA2825435863
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Lys599Arg
CA033543
NM_001077183.3:c.1796A>G