Canonical Allele Identifier: PA106456
Gene: PGM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 133287
ClinVar RCV Id: RCV000119800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002624.2:p.Asn38Tyr
CA156391
NM_002633.3:c.112A>T