Canonical Allele Identifier: PA2827009621
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535914
ClinVar RCV Id: RCV000644143 RCV002331187
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Asn1373Ser
CA276753586
NM_001318829.2:c.4118A>G