Canonical Allele Identifier: PA2827931718
Gene: PFKM HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341670.1:p.Arg47Pro
CA114800
NM_001354741.2:c.140G>C