Canonical Allele Identifier: PA2827020172
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65219
ClinVar RCV Id: RCV000055439

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Asp1479Ala
CA020755
NM_001318832.2:c.4436A>C