Canonical Allele Identifier: PA2827010464
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2858176
ClinVar RCV Id: RCV003626158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Gln1637Arg
CA394314795
NM_001318829.2:c.4910A>G