Allele Registry

Canonical Allele Identifier: PA2826483001

Gene: LY9 HGNC NCBI

ClinVar Allele:

1230885

ClinVar RCV:

RCV001641434

ClinVar Variation:

1242630

HGVS (amino-acid)	Matching Registered Transcripts
NP_001248385.1:p.Met588Val	CA1202003 NM_001261456.1:c.1762A>G