Canonical Allele Identifier: PA2825576031
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49522
ClinVar RCV Id: RCV000042782 RCV000541237 RCV000764029 RCV001021518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Asp1296Val
CA019742
NM_001114382.3:c.3887A>T