Canonical Allele Identifier: PA658667066
Gene: RAPSN HGNC NCBI

Linked Data

ClinVar Variation Id: 476125
ClinVar RCV Id: RCV000553703 RCV001274410 RCV001556490
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005046.2:p.Arg259His
CA5976642
NM_005055.5:c.776G>A