Canonical Allele Identifier: PA916023656
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 318315

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ile617Val
CA033640
NM_001318832.2:c.1849A>G