Allele Registry

Canonical Allele Identifier: PA2826701752

Gene: RAB30 HGNC NCBI

ClinVar RCV:

RCV004230202

ClinVar Variation:

2392762

HGVS (amino-acid)	Matching Registered Transcripts
NP_001272990.1:p.Ala18Gly	CA382188214 NM_001286061.1:c.53C>G