Canonical Allele Identifier: PA2580543978
Gene: RP1L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1901167
ClinVar RCV Id: RCV002586193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849188.4:p.Pro151Arg
CA171954679
NM_178857.5:c.452C>G