ClinGen Allele Registry
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Canonical Allele Identifier:
PA2829979085
Gene: TSC2
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000043356
RCV000228930
RCV000567364
RCV001699111
RCV001727553
RCV004537179
ClinVar Variation:
50090
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_066399.2:p.Ala1121Val
CA019211
NM_021055.3:c.3362C>T