Canonical Allele Identifier: PA2827929896
Gene: PFKM HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341666.1:p.Arg110Pro
CA114800
NM_001354737.1:c.329G>C