Canonical Allele Identifier: PA2825434117
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 486639

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Gly33Ser
CA056868
NM_001077183.3:c.97G>A