Allele Registry

Canonical Allele Identifier: PA2825461249

Gene: CNGA3 HGNC NCBI

ClinVar RCV:

RCV000010086

RCV000415000

RCV001002970

RCV001055558

RCV001074686

RCV001942579

ClinVar Variation:

9478

1365127

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073347.1:p.Phe529Leu	CA254823 NM_001079878.2:c.1587C>A CA347833975 NM_001079878.2:c.1585T>C CA347833980 NM_001079878.2:c.1587C>G