Canonical Allele Identifier: PA2827020924
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_001305761.1:p.Asp1678Gly
CA16614798
NM_001318832.2:c.5033A>G