Canonical Allele Identifier: PA270028
Gene: CRX HGNC NCBI

Linked Data

ClinVar Variation Id: 143085

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000545.1:p.Asp65His
CA270027
NM_000554.6:c.193G>C