Canonical Allele Identifier: PA2829978192
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2564646
ClinVar RCV Id: RCV003297078

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Gly1005Asp
CA394285202
NM_021055.3:c.3014G>A