Canonical Allele Identifier: PA2580484496
Gene: RAPSN HGNC NCBI

Linked Data

ClinVar Variation Id: 2216094
ClinVar RCV Id: RCV002665604
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116034.2:p.Gly240Arg
CA5976657
NM_032645.5:c.718G>A
CA380330388
NM_032645.5:c.718G>C