Canonical Allele Identifier: PA645393189
Gene: CRX HGNC NCBI

Linked Data

ClinVar Variation Id: 329693

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000545.1:p.His10Asp
CA9544368
NM_000554.6:c.28C>G