Allele Registry

Canonical Allele Identifier: PA2827931626

Gene: PFKM HGNC NCBI

ClinVar RCV:

RCV000001218

ClinVar Variation:

1159

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341669.1:p.Trp734Cys	CA114809 NM_001354740.1:c.2202G>T CA384555857 NM_001354740.1:c.2202G>C