Canonical Allele Identifier: PA2825956689
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466056

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Lys615Arg
CA375362211
NM_001162427.2:c.1844A>G