Canonical Allele Identifier: PA2827073919
Gene: EXOC6B HGNC NCBI

Linked Data

ClinVar Variation Id: 1991454
ClinVar RCV Id: RCV002790633
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308659.1:p.Ile448Val
CA347429679
NM_001321730.2:c.1342A>G