Canonical Allele Identifier: PA2829551549
Gene: RAB27A HGNC NCBI

Linked Data

ClinVar Variation Id: 2048141
ClinVar RCV Id: RCV002918574
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004571.2:p.Met119Val
CA270729443
NM_004580.5:c.355A>G