Canonical Allele Identifier: PA2573241435
Gene: RAPSN HGNC NCBI

Linked Data

ClinVar Variation Id: 1518617
ClinVar RCV Id: RCV002023992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005046.2:p.Arg282Leu
CA380329342
NM_005055.5:c.845G>T