Canonical Allele Identifier: PA2829551566
Gene: RAB27A HGNC NCBI

Linked Data

ClinVar Variation Id: 3150657
ClinVar RCV Id: RCV004443064
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004571.2:p.Gln140His
CA392529647
NM_004580.5:c.420G>T
CA392529648
NM_004580.5:c.420G>C