Canonical Allele Identifier: PA2827016742
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65284
ClinVar RCV Id: RCV000055506 RCV003512008
ClinVar Variation Id: 593812
ClinVar RCV Id: RCV000728954
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Met12Ile
CA019804
NM_001318832.2:c.36G>A
CA394300412
NM_001318832.2:c.36G>C
CA394300423
NM_001318832.2:c.36G>T