Allele Registry

Canonical Allele Identifier: PA117891

Gene: RAB27A HGNC NCBI

ClinVar RCV:

RCV000006352

ClinVar Variation:

5986

HGVS (amino-acid)	Matching Registered Transcripts
NP_899058.1:p.Leu130Pro	CA117889 NM_183235.3:c.389T>C