Canonical Allele Identifier: PA2827930810
Gene: PFKM HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341668.1:p.Arg110Leu
CA114804
NM_001354739.1:c.329G>T