Canonical Allele Identifier: PA891853691
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 574061
ClinVar RCV Id: RCV000695896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg1751Pro
CA394314761
NM_000548.5:c.5252G>C