Canonical Allele Identifier: PA2827010459
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207760

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Arg1636His
CA054581
NM_001318829.2:c.4907G>A