Allele Registry

Canonical Allele Identifier: PA136663

Gene: GPSM2 HGNC NCBI

ClinVar RCV:

RCV000038780

RCV000333660

RCV000992088

ClinVar Variation:

45564

HGVS (amino-acid)	Matching Registered Transcripts
NP_037428.3:p.Thr457Met	CA136662 NM_013296.5:c.1370C>T