ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA645430037
Gene: STX11
HGNC
NCBI
Linked Data
ClinVar RCV:
RCV000269130
RCV000692657
RCV002263648
ClinVar Variation:
355597
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_003755.2:p.Leu9del
CA4031597
NM_003764.4:c.24_26del