Allele Registry

Canonical Allele Identifier: PA2828100747

Gene: PFKM HGNC NCBI

ClinVar RCV:

RCV000001218

ClinVar Variation:

1159

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350548.1:p.Trp655Cys	CA114809 NM_001363619.2:c.1965G>T CA384555857 NM_001363619.2:c.1965G>C