Canonical Allele Identifier: PA2827010376
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49867

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Arg1614Cys
CA022096
NM_001318829.2:c.4840C>T