Canonical Allele Identifier: PA195055
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 186511

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Asn1008Lys
CA007132
NM_000368.5:c.3024T>G
CA375367845
NM_000368.5:c.3024T>A