ClinGen Allele Registry
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Canonical Allele Identifier:
PA2829983010
Gene: TSC2
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000189942
RCV000473026
RCV000570790
RCV003996872
RCV004537592
ClinVar Variation:
207692
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_066399.2:p.Val1656Met
CA053941
NM_021055.3:c.4966G>A