Canonical Allele Identifier: PA2825437789
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406092

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Gln1185Arg
CA16614724
NM_001077183.3:c.3554A>G