Canonical Allele Identifier: PA2827932625
Gene: PFKM HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341672.1:p.Arg39Pro
CA114800
NM_001354743.2:c.116G>C