Allele Registry

Canonical Allele Identifier: PA2827676735

Gene: ARMC9 HGNC NCBI

ClinVar RCV:

RCV000490913

RCV000515485

RCV001034541

ClinVar Variation:

427936

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339687.2:p.Pro487Leu	CA350957057 NM_001352758.2:c.1460C>T