Canonical Allele Identifier: PA107818
Gene: PFKM HGNC NCBI
ClinVar RCV:
RCV000001213
ClinVar Variation:
1154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000280.1:p.Arg39Pro
CA114800
NM_000289.5:c.116G>C