Canonical Allele Identifier: PA2573199973
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1386739
ClinVar RCV Id: RCV001905856
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Ala618Gly
CA394272985
NM_001318832.2:c.1853C>G