Canonical Allele Identifier: PA2827018580
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 452351
ClinVar RCV Id: RCV000521882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Thr1026Ser
CA394285482
NM_001318832.2:c.3076A>T
CA394285499
NM_001318832.2:c.3077C>G