Canonical Allele Identifier: PA2827003168
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_001305756.1:p.Thr977Asn
CA394285444
NM_001318827.2:c.2930C>A