Canonical Allele Identifier: PA2828421467
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535944
ClinVar RCV Id: RCV000644178
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Asp1647Asn
CA394311729
NM_001370405.1:c.4939G>A