Canonical Allele Identifier: PA2825957997
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411281

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Asp1056Asn
CA16612730
NM_001162427.2:c.3166G>A