Canonical Allele Identifier: PA2827929596
Gene: PFKM HGNC NCBI

Linked Data

ClinVar Variation Id: 1326057
ClinVar RCV Id: RCV001786118 RCV002541237
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341665.1:p.Arg191Trp
CA6536952
NM_001354736.1:c.571C>T