Canonical Allele Identifier: PA2573309286
Gene: RP1L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1419489
ClinVar RCV Id: RCV001910391
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849188.4:p.Val169Ala
CA4625664
NM_178857.5:c.506T>C