Canonical Allele Identifier: PA1139762322
Gene: RP1L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 866377

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849188.4:p.Gly201Arg
CA4625628
NM_178857.5:c.601G>A
CA370299683
NM_178857.5:c.601G>C