Canonical Allele Identifier: PA2828410044
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207698

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Val109Met
CA045030
NM_001370404.1:c.325G>A