Canonical Allele Identifier: PA107911
Gene: PGAM2 HGNC NCBI
ClinVar RCV:
RCV000000447
ClinVar Variation:
419
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000281.2:p.Glu89Ala
CA114260
NM_000290.4:c.266A>C