Canonical Allele Identifier: PA2829551550
Gene: RAB27A HGNC NCBI

Linked Data

ClinVar Variation Id: 536460
ClinVar RCV Id: RCV000644916

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004571.2:p.Tyr122Phe
CA392529856
NM_004580.5:c.365A>T