Canonical Allele Identifier: PA2828415907
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535934

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Arg25Lys
CA056318
NM_001370405.1:c.74G>A