Canonical Allele Identifier: PA107891
Gene: PFKM HGNC NCBI
ClinVar RCV:
RCV000001218
ClinVar Variation:
1159
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000280.1:p.Trp686Cys
CA114809
NM_000289.5:c.2058G>T
CA384555857
NM_000289.5:c.2058G>C