Canonical Allele Identifier: PA2827010587
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2884748
ClinVar RCV Id: RCV003626577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Glu1668Asp
CA394315728
NM_001318829.2:c.5004G>T
CA394315730
NM_001318829.2:c.5004G>C