Canonical Allele Identifier: PA2825186787
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2506402
ClinVar RCV Id: RCV003234985

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Gly1408Asp
CA394300149
NM_000548.5:c.4223G>A