Canonical Allele Identifier: PA2829576337
Gene: RAPSN HGNC NCBI

Linked Data

ClinVar Variation Id: 3236670
ClinVar RCV Id: RCV004556130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005046.2:p.Arg268Met
CA380329772
NM_005055.5:c.803G>T