Canonical Allele Identifier: PA109371
Gene: CRX HGNC NCBI

Linked Data

ClinVar Variation Id: 7421
ClinVar RCV Id: RCV000007846 RCV000085990 RCV001075469 RCV001059718
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000545.1:p.Arg41Gln
CA118791
NM_000554.6:c.122G>A