Canonical Allele Identifier: PA2827010424
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Arg1628Pro
CA022224
NM_001318829.2:c.4883G>C