Canonical Allele Identifier: PA136669
Gene: GPSM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 45568
ClinVar RCV Id: RCV000038784 RCV000398884 RCV002054716
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_037428.3:p.Arg127Gln
CA136668
NM_013296.5:c.380G>A