Canonical Allele Identifier: PA916052637
Gene: RAB27A HGNC NCBI

Linked Data

ClinVar Variation Id: 640213
ClinVar RCV Id: RCV000793188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_899059.1:p.Gly32Arg
CA7573706
NM_183236.3:c.94G>C