ClinGen Allele Registry
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Canonical Allele Identifier:
PA2828558838
Gene: FAM111A
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1361113
ClinVar RCV Id:
RCV001865115
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001361782.1:p.Ile572del
CA6016823
NM_001374853.1:c.1713_1715del
CA6016824
NM_001374853.1:c.1714_1716del