Canonical Allele Identifier: PA2828731763
Gene: RPGRIP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1900288
ClinVar RCV Id: RCV002582971 RCV002576442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001364877.1:p.Val325Met
CA257536068
NM_001377948.1:c.973G>A