Canonical Allele Identifier: PA2573090181
Gene: GPSM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1304803
ClinVar RCV Id: RCV001765039

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_037428.3:p.Arg405Cys
CA982999
NM_013296.5:c.1213C>T