Allele Registry

Canonical Allele Identifier: PA916055943

Gene: ARMC9 HGNC NCBI

ClinVar RCV:

RCV000490882

RCV000515503

RCV001034533

ClinVar Variation:

427939

HGVS (amino-acid)	Matching Registered Transcripts
NP_079415.4:p.Arg446Cys	CA2160301 NM_025139.6:c.1336C>T