Canonical Allele Identifier: PA2825956760
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 48880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Gly630Ser
CA005830
NM_001162427.2:c.1888G>A