Canonical Allele Identifier: PA2828091561
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.His600Tyr
CA033559
NM_001363528.2:c.1798C>T