Canonical Allele Identifier: PA2828091839
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2564616
ClinVar RCV Id: RCV003297048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Pro669Ser
CA394274452
NM_001363528.2:c.2005C>T