Canonical Allele Identifier: PA916039335
Gene: PFKM HGNC NCBI
ClinVar RCV:
RCV000001213
ClinVar Variation:
1154
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341669.1:p.Arg87Pro
CA114800
NM_001354740.1:c.260G>C