Allele Registry

Canonical Allele Identifier: PA2827932076

Gene: PFKM HGNC NCBI

ClinVar RCV:

RCV000001218

ClinVar Variation:

1159

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341670.1:p.Trp694Cys	CA114809 NM_001354741.2:c.2082G>T CA384555857 NM_001354741.2:c.2082G>C