Canonical Allele Identifier: PA2827003382
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_001305756.1:p.Met1051Val
CA16614772
NM_001318827.2:c.3151A>G