Canonical Allele Identifier: PA117894
Gene: RAB27A HGNC NCBI

Linked Data

ClinVar Variation Id: 5987
ClinVar RCV Id: RCV000006353
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_899058.1:p.Ala152Pro
CA117892
NM_183235.3:c.454G>C