Canonical Allele Identifier: PA2825577188
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49978
ClinVar RCV Id: RCV000043245 RCV001238557 RCV002345329
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Gly1619Asp
CA021290
NM_001114382.3:c.4856G>A