Canonical Allele Identifier: PA2827933522
Gene: PFKM HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341674.1:p.Arg10Pro
CA114800
NM_001354745.2:c.29G>C