Allele Registry

Canonical Allele Identifier: PA2499261077

Gene: LY9 HGNC NCBI

ClinVar RCV:

RCV001641434

ClinVar Variation:

1242630

HGVS (amino-acid)	Matching Registered Transcripts
NP_002339.2:p.Met602Val	CA1202003 NM_002348.4:c.1804A>G