Canonical Allele Identifier: PA2827007277
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207722

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Lys550Arg
CA033543
NM_001318829.2:c.1649A>G