Canonical Allele Identifier: PA2825576362
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 579558

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ser1388Asn
CA394300256
NM_001114382.3:c.4163G>A