Canonical Allele Identifier: PA2827068211
Gene: GPSM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 505415
ClinVar RCV Id: RCV000603703 RCV001101471
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307968.1:p.Ala345Gly
CA341464974
NM_001321039.3:c.1034C>G