Canonical Allele Identifier: PA645388478
Gene: GPSM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 291700
ClinVar RCV Id: RCV000290642

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_037428.3:p.Arg93Lys
CA982755
NM_013296.5:c.278G>A