Canonical Allele Identifier: PA2826034904
Gene: PFKM HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160160.1:p.Arg39Pro
CA114800
NM_001166688.2:c.116G>C