Canonical Allele Identifier: PA2830086020
Gene: RAPSN HGNC NCBI

Linked Data

ClinVar Variation Id: 542733
ClinVar RCV Id: RCV000653215 RCV001835896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116034.2:p.Arg278Cys
CA380327816
NM_032645.5:c.832C>T