Canonical Allele Identifier: PA915987472
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Ser978Asn
CA319258
NM_001162427.2:c.2933G>A