Canonical Allele Identifier: PA658805576
Gene: RAB3GAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 100771
ClinVar RCV Id: RCV000087135
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036365.1:p.Thr18Pro
CA150637
NM_012233.3:c.52A>C