Canonical Allele Identifier: PA2580544001
Gene: RP1L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2054491
ClinVar RCV Id: RCV002909794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849188.4:p.Gly183Cys
CA4625649
NM_178857.5:c.547G>T