Canonical Allele Identifier: PA2828414526
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Gly1428Ser
CA051085
NM_001370404.1:c.4282G>A