Canonical Allele Identifier: PA2827001901
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207723

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Arg602Trp
CA034455
NM_001318827.2:c.1804C>T