Canonical Allele Identifier: PA2825313972
Gene: RGR HGNC NCBI

Linked Data

ClinVar Variation Id: 9181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001012740.1:p.Ser66Arg
CA241383
NM_001012722.2:c.196A>C
CA377390864
NM_001012722.2:c.198C>A
CA377390865
NM_001012722.2:c.198C>G