Canonical Allele Identifier: PA2827009589
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Asp1363Asn
CA394302242
NM_001318829.2:c.4087G>A