Allele Registry

Canonical Allele Identifier: PA114810

Gene: PFKM HGNC NCBI

ClinVar RCV:

RCV000001218

ClinVar Variation:

1159

HGVS (amino-acid)	Matching Registered Transcripts
NP_001160158.1:p.Trp757Cys	CA114809 NM_001166686.2:c.2271G>T CA384555857 NM_001166686.2:c.2271G>C