Canonical Allele Identifier: PA2828421613
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1025177
ClinVar RCV Id: RCV001325462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Asn1684Ser
CA054360
NM_001370405.1:c.5051A>G