Canonical Allele Identifier: PA2827008286
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 318323

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Lys896Arg
CA10648020
NM_001318829.2:c.2687A>G