Canonical Allele Identifier: PA2827007251
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 509382

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ser543Asn
CA033474
NM_001318829.2:c.1628G>A