Canonical Allele Identifier: PA645391176
Gene: RAB27A HGNC NCBI

Linked Data

ClinVar Variation Id: 436459
ClinVar RCV Id: RCV000501657 RCV002263710
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_899058.1:p.Met1Thr