Canonical Allele Identifier: PA2828418111
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535965
ClinVar RCV Id: RCV000644209 RCV002255485 RCV004004014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Pro674Ser
CA035778
NM_001370405.1:c.2020C>T