Allele Registry

Canonical Allele Identifier: PA2827934729

Gene: PFKM HGNC NCBI

ClinVar RCV:

RCV000001218

ClinVar Variation:

1159

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341676.1:p.Trp636Cys	CA114809 NM_001354747.2:c.1908G>T CA384555857 NM_001354747.2:c.1908G>C