Canonical Allele Identifier: PA2827931176
Gene: PFKM HGNC NCBI

Linked Data

ClinVar Variation Id: 1159
ClinVar RCV Id: RCV000001218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341668.1:p.Trp757Cys
CA114809
NM_001354739.1:c.2271G>T
CA384555857
NM_001354739.1:c.2271G>C