Allele Registry

Canonical Allele Identifier: PA645388586

Gene: RP1L1 HGNC NCBI

ClinVar Variation Id: 424192

HGVS (amino-acid)	Matching Registered Transcripts
NP_849188.4:p.Gly1711Ala	CA4623757 NM_178857.5:c.5132G>C