Canonical Allele Identifier: PA2827020028
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65206
ClinVar RCV Id: RCV000055424 RCV001230160 RCV003332112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Pro1441Ser
CA020513
NM_001318832.2:c.4321C>T