Canonical Allele Identifier: PA206093
Gene: RAB3GAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 211989
ClinVar RCV Id: RCV000192933 RCV000638451 RCV001096880 RCV001096881 RCV001721259 RCV004530142
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036546.2:p.Ile1354Val
CA206092
NM_012414.4:c.4060A>G