Canonical Allele Identifier: PA2827017706
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1774028

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Asp512Asn
CA394326047
NM_001318832.2:c.1534G>A