Canonical Allele Identifier: PA2580321160
Gene: RAPSN HGNC NCBI

Linked Data

ClinVar Variation Id: 2078869
ClinVar RCV Id: RCV002988858 RCV003134578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005046.2:p.Asp303Glu
CA5976593
NM_005055.5:c.909C>G
CA380328845
NM_005055.5:c.909C>A