Canonical Allele Identifier: PA2828061085
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 186511

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Asn887Lys
CA007132
NM_001362177.1:c.2661T>G
CA375367845
NM_001362177.1:c.2661T>A