Canonical Allele Identifier: PA2826944830
Gene: FAM111A HGNC NCBI

Linked Data

ClinVar Variation Id: 56810
ClinVar RCV Id: RCV000050209 RCV000419087 RCV000988563 RCV001249420 RCV001267015
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001299839.1:p.Arg569His
CA344770
NM_001312910.2:c.1706G>A