Canonical Allele Identifier: PA2828417720
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535878
ClinVar RCV Id: RCV000644096 RCV002493022 RCV004025654
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ala580Gly
CA033236
NM_001370405.1:c.1739C>G