Canonical Allele Identifier: PA2828560774
Gene: FAM111A HGNC NCBI

Linked Data

ClinVar Variation Id: 2574550
ClinVar RCV Id: RCV003319132
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361791.1:p.Phe536Leu
CA380789249
NM_001374862.1:c.1606T>C
CA380789273
NM_001374862.1:c.1608T>A
CA380789277
NM_001374862.1:c.1608T>G