Canonical Allele Identifier: PA658806412
Gene: GPSM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 505415
ClinVar RCV Id: RCV000603703 RCV001101471
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_037428.3:p.Ala345Gly
CA341464974
NM_013296.5:c.1034C>G