Canonical Allele Identifier: PA1139675609
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 975118
ClinVar RCV Id: RCV001251523
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030025.1:p.Gly921Arg
CA412729843
NM_001034853.2:c.2761G>C
CA412729844
NM_001034853.2:c.2761G>A