Canonical Allele Identifier: PA2580544087
Gene: RP1L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2466629

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849188.4:p.Gly399Arg
CA4625273
NM_178857.5:c.1195G>A
CA370296050
NM_178857.5:c.1195G>C