Canonical Allele Identifier: PA206884
Gene: RAB3GAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 211984
ClinVar RCV Id: RCV000193412 RCV000299268 RCV000393027 RCV000877111 RCV001705085
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036546.2:p.Leu670Val
CA206883
NM_012414.4:c.2008C>G