Canonical Allele Identifier: PA2827010572
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 514715

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Gln1664Arg
CA055149
NM_001318829.2:c.4991A>G