Allele Registry

Canonical Allele Identifier: PA117888

Gene: RAB27A HGNC NCBI

ClinVar RCV:

RCV000006348

ClinVar Variation:

5982

HGVS (amino-acid)	Matching Registered Transcripts
NP_899058.1:p.Trp73Gly	CA117886 NM_183235.3:c.217T>G