Canonical Allele Identifier: PA2828559053
Gene: FAM111A HGNC NCBI

Linked Data

ClinVar Variation Id: 56810

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361783.1:p.Arg569His
CA344770
NM_001374854.1:c.1706G>A