Canonical Allele Identifier: PA2825436931
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135375

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Leu921Val
CA018107
NM_001077183.3:c.2761C>G