Canonical Allele Identifier: PA645492812
Gene: RAB3GAP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 295638
ClinVar RCV Id: RCV000305520 RCV000360283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036546.2:p.Glu1326Asp
CA10609219
NM_012414.4:c.3978G>T
CA344624548
NM_012414.4:c.3978G>C