Allele Registry

Canonical Allele Identifier: PA2826035269

Gene: PFKM HGNC NCBI

ClinVar RCV:

RCV000001218

ClinVar Variation:

1159

HGVS (amino-acid)	Matching Registered Transcripts
NP_001160160.1:p.Trp686Cys	CA114809 NM_001166688.2:c.2058G>T CA384555857 NM_001166688.2:c.2058G>C