Canonical Allele Identifier: PA2573254674
Gene: GPSM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1365343
ClinVar RCV Id: RCV001911900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_037428.3:p.Arg573His
CA341451543
NM_013296.5:c.1718G>A