Canonical Allele Identifier: PA112298
Gene: FMO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 16314
ClinVar RCV Id: RCV000017707 RCV003556037
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001002294.1:p.Met434Ile
CA257488
NM_001002294.3:c.1302G>A
CA343169771
NM_001002294.3:c.1302G>C
CA343169774
NM_001002294.3:c.1302G>T