Canonical Allele Identifier: PA2827067996
Gene: GPSM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 499162
ClinVar RCV Id: RCV000598197 RCV000726962
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307967.1:p.Leu496Ile
CA983071
NM_001321038.2:c.1486T>A