Allele Registry

Canonical Allele Identifier: PA2827676844

Gene: ARMC9 HGNC NCBI

ClinVar RCV:

RCV000491981

RCV000515488

RCV001034532

RCV001362306

ClinVar Variation:

427930

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339688.2:p.Gly69Arg	CA2159877 NM_001352759.2:c.205G>A CA350945883 NM_001352759.2:c.205G>C