Canonical Allele Identifier: PA2827068319
Gene: GPSM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2173455
ClinVar RCV Id: RCV002581917 RCV003274246
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307968.1:p.Arg573Cys
CA983156
NM_001321039.3:c.1717C>T