Canonical Allele Identifier: PA2825576098
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406097
ClinVar RCV Id: RCV000473934 RCV002323695
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ser1311Asn
CA16615016
NM_001114382.3:c.3932G>A