Canonical Allele Identifier: PA109395
Gene: CRX HGNC NCBI

Linked Data

ClinVar Variation Id: 7422
ClinVar RCV Id: RCV000007847 RCV000086364 RCV001244346 RCV001074643
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000545.1:p.Arg90Trp
CA118792
NM_000554.6:c.268C>T