Canonical Allele Identifier: PA227625
Gene: CRX HGNC NCBI

Linked Data

ClinVar Variation Id: 99605
ClinVar RCV Id: RCV000086001 RCV000787829 RCV000990235 RCV001089193 RCV001131568 RCV001257854 RCV001131569
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000545.1:p.Tyr142Cys
CA227624
NM_000554.6:c.425A>G