Canonical Allele Identifier: PA2825435249
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Glu405Gln
CA028805
NM_001077183.3:c.1213G>C