Canonical Allele Identifier: PA2827068108
Gene: GPSM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 45568
ClinVar RCV Id: RCV000038784 RCV000398884 RCV002054716
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307968.1:p.Arg127Gln
CA136668
NM_001321039.3:c.380G>A