Allele Registry

Canonical Allele Identifier: PA117900

Gene: RAB27A HGNC NCBI

ClinVar RCV:

RCV000006357

RCV000169674

RCV000524022

ClinVar Variation:

5991

HGVS (amino-acid)	Matching Registered Transcripts
NP_004571.2:p.Ala87Pro	CA117898 NM_004580.5:c.259G>C