Canonical Allele Identifier: PA645387859
Gene: RP1L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 361410
ClinVar RCV Id: RCV000344029 RCV002058690
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849188.4:p.Ser143Phe
CA4625706
NM_178857.5:c.428C>T