Canonical Allele Identifier: PA2825576595
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Asp1455Asn
CA394302242
NM_001114382.3:c.4363G>A