Canonical Allele Identifier: PA2827931626
Gene: PFKM HGNC NCBI

Linked Data

ClinVar Variation Id: 1159
ClinVar RCV Id: RCV000001218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341669.1:p.Trp734Cys
CA114809
NM_001354740.1:c.2202G>T
CA384555857
NM_001354740.1:c.2202G>C