Canonical Allele Identifier: PA2499231732
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1059231

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Asn859Ser
CA375370037
NM_000368.5:c.2576A>G