Canonical Allele Identifier: PA2827010425
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49471

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Arg1628Trp
CA022213
NM_001318829.2:c.4882C>T