Canonical Allele Identifier: PA645492666
Gene: RAB3GAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 235683
ClinVar RCV Id: RCV000224837 RCV000347930 RCV000528699 RCV000283527 RCV000502830 RCV004541363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036546.2:p.Leu764Phe
CA1402470
NM_012414.4:c.2290C>T