Canonical Allele Identifier: PA2825956738
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207613

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Trp625Arg
CA030669
NM_001162427.2:c.1873T>A
CA375361293
NM_001162427.2:c.1873T>C