Allele Registry

Canonical Allele Identifier: PA2826483040

Gene: LY9 HGNC NCBI

ClinVar Allele:

1230885

ClinVar RCV:

RCV001641434

ClinVar Variation:

1242630

HGVS (amino-acid)	Matching Registered Transcripts
NP_001248386.1:p.Met512Val	CA1202003 NM_001261457.1:c.1534A>G