Allele Registry

Canonical Allele Identifier: PA2827675604

Gene: ARMC9 HGNC NCBI

ClinVar RCV:

RCV000491717

RCV000515505

RCV001034537

RCV001038181

RCV001257947

ClinVar Variation:

427932

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339684.2:p.Arg343Cys	CA2160165 NM_001352755.2:c.1027C>T