Canonical Allele Identifier: PA2828094651
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3232172
ClinVar RCV Id: RCV004520855
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Gly1485Ala
CA394305032
NM_001363528.2:c.4454G>C