Canonical Allele Identifier: PA2828413365
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406099
ClinVar RCV Id: RCV000473877 RCV001020177 RCV000509526 RCV001584141 RCV004000718 RCV003463869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Met1087Val
CA16614772
NM_001370404.1:c.3259A>G