Canonical Allele Identifier: PA2580353743
Gene: RP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2086950
ClinVar RCV Id: RCV003007743

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_008846.2:p.Pro95His
CA413039192
NM_006915.3:c.284C>A