Canonical Allele Identifier: PA645387836
Gene: RP1L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 361419
ClinVar RCV Id: RCV000354066 RCV002523621
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849188.4:p.Ala92Val
CA10629898
NM_178857.5:c.275C>T