Canonical Allele Identifier: PA645413182
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411260

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.His371Gln
CA027069
NM_000368.5:c.1113C>A
CA375367436
NM_000368.5:c.1113C>G