Canonical Allele Identifier: PA2826034812
Gene: PFKM HGNC NCBI

Linked Data

ClinVar Variation Id: 1159
ClinVar RCV Id: RCV000001218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160159.1:p.Trp686Cys
CA114809
NM_001166687.2:c.2058G>T
CA384555857
NM_001166687.2:c.2058G>C