Canonical Allele Identifier: PA2825795634
Gene: FAM111A HGNC NCBI

Linked Data

ClinVar Variation Id: 1361113
ClinVar RCV Id: RCV001865115
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001135991.1:p.Ile572del
CA6016823
NM_001142519.3:c.1713_1715del
CA6016824
NM_001142519.3:c.1714_1716del