Canonical Allele Identifier: PA2827009823
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 825059
ClinVar RCV Id: RCV001022821 RCV001066426
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Ala1431Thr
CA394304918
NM_001318829.2:c.4291G>A