Canonical Allele Identifier: PA2825955917
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411263

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Gly401Ala
CA028454
NM_001162427.2:c.1202G>C