Canonical Allele Identifier: PA2827933523
Gene: PFKM HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341674.1:p.Arg10Leu
CA114804
NM_001354745.2:c.29G>T