ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA111314
Gene: INF2
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1053
ClinVar RCV Id:
RCV000001108
RCV001380435
RCV002293971
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_071934.3:p.Arg214His
CA114725
NM_022489.4:c.641G>A