Canonical Allele Identifier: PA2827934188
Gene: PFKM HGNC NCBI

Linked Data

ClinVar Variation Id: 526619
ClinVar Variation Id: 618271

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341675.1:p.Gln405Lys
CA6537312
NM_001354746.2:c.1213C>A
CA658797898
NM_001354746.2:c.1212_1213delinsAA