Canonical Allele Identifier: PA227618
Gene: CRX HGNC NCBI

Linked Data

ClinVar Variation Id: 99599
ClinVar RCV Id: RCV000085994 RCV001003002 RCV001854500
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000545.1:p.Glu80Lys
CA227617
NM_000554.6:c.238G>A