Canonical Allele Identifier: PA658805813
Gene: RAPSN HGNC NCBI

Linked Data

ClinVar Variation Id: 497298
ClinVar RCV Id: RCV000591406 RCV000855473 RCV001867917 RCV003465332
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005046.2:p.Arg91Leu
CA5976768
NM_005055.5:c.272G>T