Canonical Allele Identifier: PA154875
Gene: RAPSN HGNC NCBI

Linked Data

ClinVar Variation Id: 130090
ClinVar RCV Id: RCV000118118 RCV000311015 RCV000390783 RCV001521377 RCV001538027 RCV001275252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005046.2:p.Arg58Cys
CA154874
NM_005055.5:c.172C>T