Canonical Allele Identifier: PA2825436459
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 281384

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Ala765Val
CA10603864
NM_001077183.3:c.2294C>T