Canonical Allele Identifier: PA2825576946
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535941
ClinVar RCV Id: RCV000644175

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Tyr1548His
CA394307381
NM_001114382.3:c.4642T>C