Canonical Allele Identifier: PA2827068130
Gene: GPSM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 178375
ClinVar RCV Id: RCV000155122 RCV002514984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307968.1:p.Arg198Gln
CA182210
NM_001321039.3:c.593G>A