Canonical Allele Identifier: PA913196893
Gene: FAM111A HGNC NCBI

Linked Data

ClinVar Variation Id: 56810

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071357.2:p.Arg569His
CA344770
NM_022074.4:c.1706G>A