Canonical Allele Identifier: PA2827934729
Gene: PFKM HGNC NCBI

Linked Data

ClinVar Variation Id: 1159
ClinVar RCV Id: RCV000001218
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341676.1:p.Trp636Cys
CA114809
NM_001354747.2:c.1908G>T
CA384555857
NM_001354747.2:c.1908G>C