Canonical Allele Identifier: PA2828413102
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2449956
ClinVar RCV Id: RCV003171890 RCV003778996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Thr1013Asn
CA394285444
NM_001370404.1:c.3038C>A