Canonical Allele Identifier: PA2828409889
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65108

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ile64Val
CA016191
NM_001370404.1:c.190A>G