Canonical Allele Identifier: PA2825576705
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535877

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ser1484Tyr
CA051496
NM_001114382.3:c.4451C>A