Canonical Allele Identifier: PA2580358532
Gene: GPSM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2173455
ClinVar RCV Id: RCV002581917 RCV003274246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_037428.3:p.Arg573Cys
CA983156
NM_013296.5:c.1717C>T