Canonical Allele Identifier: PA136671
Gene: GPSM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 45569
ClinVar RCV Id: RCV000038785 RCV001099470
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_037428.3:p.Ala177Thr
CA136670
NM_013296.5:c.529G>A