Canonical Allele Identifier: PA645413262
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411248

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.His606Gln
CA029913
NM_000368.5:c.1818T>A
CA375363314
NM_000368.5:c.1818T>G