Canonical Allele Identifier: PA107924
Gene: PGAM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 421

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000281.2:p.Gly97Asp
CA114262
NM_000290.4:c.290G>A