Canonical Allele Identifier: PA658808838
Gene: RAB27A HGNC NCBI

Linked Data

ClinVar Variation Id: 536460
ClinVar RCV Id: RCV000644916

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_899058.1:p.Tyr122Phe
CA392529856
NM_183235.3:c.365A>T