Canonical Allele Identifier: PA2829551471
Gene: RAB27A HGNC NCBI

Linked Data

ClinVar Variation Id: 1058396
ClinVar RCV Id: RCV001367530
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004571.2:p.Thr41Ala
CA392530823
NM_004580.5:c.121A>G