Canonical Allele Identifier: PA241385
Gene: RGR HGNC NCBI

Linked Data

ClinVar Variation Id: 9181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002912.2:p.Ser66Arg
CA241383
NM_002921.4:c.196A>C
CA377390864
NM_002921.4:c.198C>A
CA377390865
NM_002921.4:c.198C>G