Canonical Allele Identifier: PA645388358
Gene: RP1L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 361297
ClinVar RCV Id: RCV000315863 RCV001355893 RCV001528387 RCV001796009
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849188.4:p.Glu1324Gly
CA10629800
NM_178857.5:c.3971A>G
CA171943666
NM_178857.5:c.3971_3972delinsGG