Canonical Allele Identifier: PA2827020138
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2449973
ClinVar RCV Id: RCV003171902

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Gln1469Lys
CA051854
NM_001318832.2:c.4405C>A