Canonical Allele Identifier: PA2827933447
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_001341673.1:p.Trp686Cys
CA114809
NM_001354744.2:c.2058G>T
CA384555857
NM_001354744.2:c.2058G>C