Canonical Allele Identifier: PA2825434304
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467970

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Arg93Gln
CA394305714
NM_001077183.3:c.278G>A