Canonical Allele Identifier: PA645493152
Gene: FAM222A HGNC NCBI

Linked Data

ClinVar Variation Id: 402150
ClinVar RCV Id: RCV000454202
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116218.2:p.His95Leu
CA6779560
NM_032829.3:c.284A>T