Canonical Allele Identifier: PA107804
Gene: PFKM HGNC NCBI
ClinVar RCV:
RCV000001216
ClinVar Variation:
1157
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000280.1:p.Arg39Leu
CA114804
NM_000289.5:c.116G>T