Canonical Allele Identifier: PA114805
Gene: PFKM HGNC NCBI
ClinVar RCV:
RCV000001216
ClinVar Variation:
1157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160158.1:p.Arg110Leu
CA114804
NM_001166686.2:c.329G>T