Canonical Allele Identifier: PA105011
Gene: CYP4F22 HGNC NCBI
ClinVar RCV:
RCV000000958
ClinVar Variation:
910
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_775754.2:p.His436Asp
CA114617
NM_173483.4:c.1306C>G