Allele Registry

Canonical Allele Identifier: PA2827931176

Gene: PFKM HGNC NCBI

ClinVar RCV:

RCV000001218

ClinVar Variation:

1159

HGVS (amino-acid)	Matching Registered Transcripts
NP_001341668.1:p.Trp757Cys	CA114809 NM_001354739.1:c.2271G>T CA384555857 NM_001354739.1:c.2271G>C