Canonical Allele Identifier: PA2827067968
Gene: GPSM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1195647
ClinVar RCV Id: RCV001558812
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307967.1:p.Val399Leu
CA341468171
NM_001321038.2:c.1195G>C
CA341468172
NM_001321038.2:c.1195G>T