Canonical Allele Identifier: PA2742023218
Gene: RP1L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3028050
ClinVar RCV Id: RCV003889420

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849188.4:p.Ala429Asp
CA4625238
NM_178857.5:c.1286C>A