Canonical Allele Identifier: PA2825574863
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467957

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ala894Val
CA040893
NM_001114382.3:c.2681C>T