Canonical Allele Identifier: PA2827068014
Gene: GPSM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1436298
ClinVar RCV Id: RCV001987303
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307967.1:p.Arg557Cys
CA28579335
NM_001321038.2:c.1669C>T