Canonical Allele Identifier: PA2827004611
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 432500
ClinVar RCV Id: RCV000497607 RCV001022632 RCV001078813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Ser1404Phe
CA394302786
NM_001318827.2:c.4211C>T