Canonical Allele Identifier: PA2825572358
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535868

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Asp162Asn
CA394309028
NM_001114382.3:c.484G>A