Canonical Allele Identifier: PA1139758838
Gene: RAB27A HGNC NCBI

Linked Data

ClinVar Variation Id: 967802
ClinVar RCV Id: RCV001242800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_899059.1:p.Gly156Ala
CA7573570
NM_183236.3:c.467G>C