Canonical Allele Identifier: PA2825437785
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2497442
ClinVar RCV Id: RCV003213897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Pro1183_Leu1184del
CA2580091013
NM_001077183.3:c.3548_3553del