Canonical Allele Identifier: PA2827068002
Gene: GPSM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 517193
ClinVar RCV Id: RCV000612816 RCV000840081 RCV003117419
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307967.1:p.Thr523del
CA983088
NM_001321038.2:c.1566_1568del
CA1187888433
NM_001321038.2:c.1567_1569del