Canonical Allele Identifier: PA2827933882
Gene: PFKM HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341674.1:p.Trp657Cys
CA114809
NM_001354745.2:c.1971G>T
CA384555857
NM_001354745.2:c.1971G>C