Canonical Allele Identifier: PA2825577556
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405986
ClinVar RCV Id: RCV000470291 RCV002339130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Asp1711Gly
CA16614798
NM_001114382.3:c.5132A>G