Canonical Allele Identifier: PA645492690
Gene: RAB3GAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295643
ClinVar RCV Id: RCV000278970 RCV000343307 RCV000952485 RCV001459064 RCV004537642
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036546.2:p.His1048Arg
CA1402236
NM_012414.4:c.3143A>G