Canonical Allele Identifier: PA2828061086
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466111

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Asn887Ser
CA375367854
NM_001362177.1:c.2660A>G