Canonical Allele Identifier: PA182211
Gene: GPSM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 178375
ClinVar RCV Id: RCV000155122 RCV002514984
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_037428.3:p.Arg198Gln
CA182210
NM_013296.5:c.593G>A