Canonical Allele Identifier: PA2573309304
Gene: RP1L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1436902
ClinVar RCV Id: RCV001955369
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_849188.4:p.Thr198Met
CA4625633
NM_178857.5:c.593C>T