Canonical Allele Identifier: PA2830410348
Gene: RAB27A HGNC NCBI

Linked Data

ClinVar Variation Id: 5982
ClinVar RCV Id: RCV000006348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_899057.1:p.Trp73Gly
CA117886
NM_183234.2:c.217T>G