Canonical Allele Identifier: PA2828411715
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2564740
ClinVar RCV Id: RCV003297172
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ser609Ile
CA394272998
NM_001370404.1:c.1826G>T