Canonical Allele Identifier: PA2827075055
Gene: EXOC6B HGNC NCBI

Linked Data

ClinVar Variation Id: 2155108
ClinVar RCV Id: RCV003072167
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308662.1:p.Arg605Gly
CA1708330
NM_001321733.2:c.1813C>G