Canonical Allele Identifier: PA658659839
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Asn1008Ser
CA375367854
NM_000368.5:c.3023A>G