Canonical Allele Identifier: PA2827068272
Gene: GPSM2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1305244
ClinVar RCV Id: RCV001768451

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001307968.1:p.Arg498Gln
CA983075
NM_001321039.3:c.1493G>A