Canonical Allele Identifier: PA2825438835
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 962721
ClinVar RCV Id: RCV001236628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.[Ala1479_Gly1484del;Gly1486_Gln1487del]
CA1139664288
NM_001077183.3:c.4436_4459del