Canonical Allele Identifier: PA2827068004
Gene: GPSM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 226649
ClinVar RCV Id: RCV000218159 RCV000270361 RCV000711834 RCV001701798
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307967.1:p.Ser525del
CA983090
NM_001321038.2:c.1572_1574del
CA2646884941
NM_001321038.2:c.1573_1575del