Canonical Allele Identifier: PA2829981293
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Gly1429Ser
CA051085
NM_021055.3:c.4285G>A