Canonical Allele Identifier: PA2825956758
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466059

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Gly629Arg
CA030742
NM_001162427.2:c.1885G>A
CA375361224
NM_001162427.2:c.1885G>C