Canonical Allele Identifier: PA2580544006
Gene: RP1L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2141656
ClinVar RCV Id: RCV003060420
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849188.4:p.Ser200Thr
CA4625630
NM_178857.5:c.599G>C