Canonical Allele Identifier: PA1139762322
Gene: RP1L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 866377
ClinVar RCV Id: RCV001074309 RCV001862551 RCV002554708
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849188.4:p.Gly201Arg
CA4625628
NM_178857.5:c.601G>A
CA370299683
NM_178857.5:c.601G>C