Canonical Allele Identifier: PA2825184593
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2564646
ClinVar RCV Id: RCV003297078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Gly1048Asp
CA394285202
NM_000548.5:c.3143G>A