Canonical Allele Identifier: PA2826034241
Gene: PFKM HGNC NCBI

Linked Data

ClinVar Variation Id: 526619
ClinVar Variation Id: 618271

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160158.1:p.Gln518Lys
CA6537312
NM_001166686.2:c.1552C>A
CA658797898
NM_001166686.2:c.1551_1552delinsAA