Allele Registry

Canonical Allele Identifier: PA117894

Gene: RAB27A HGNC NCBI

ClinVar RCV:

RCV000006353

ClinVar Variation:

5987

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