Canonical Allele Identifier: PA2828409719
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230395
ClinVar RCV Id: RCV000213113 RCV000537615
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Ser6Asn
CA033570
NM_001370404.1:c.17G>A