Canonical Allele Identifier: PA645502590
Gene: RPGR HGNC NCBI

Linked Data

ClinVar Variation Id: 403392
ClinVar RCV Id: RCV000455013 RCV001591058 RCV002063668
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001030025.1:p.Asn1077Lys
CA10385168
NM_001034853.2:c.3231T>A
CA412727594
NM_001034853.2:c.3231T>G