Canonical Allele Identifier: PA2825954381
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Ser1028Asn
CA319258
NM_001162426.2:c.3083G>A