Canonical Allele Identifier: PA645294394
Gene: RAB27A HGNC NCBI

Linked Data

ClinVar Variation Id: 419794

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004571.2:p.Arg82Cys
CA7573638
NM_004580.5:c.244C>T