Canonical Allele Identifier: PA188985
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 184443

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000359.1:p.Gln527Arg
CA005092
NM_000368.5:c.1580A>G