Allele Registry

Canonical Allele Identifier: PA100864

Gene: GP9 HGNC NCBI

ClinVar RCV:

RCV000014488

RCV000177000

RCV001003901

ClinVar Variation:

13533

HGVS (amino-acid)	Matching Registered Transcripts
NP_000165.1:p.Cys24Arg	CA123181 NM_000174.5:c.70T>C