Canonical Allele Identifier: PA2827929107
Gene: PFKM HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341664.1:p.Arg142Pro
CA114800
NM_001354735.1:c.425G>C