Canonical Allele Identifier: PA174649
Gene: EXOC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 161714
ClinVar RCV Id: RCV000149250
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060773.3:p.Arg414His
CA174648
NM_018303.6:c.1241G>A