Canonical Allele Identifier: PA2580484495
Gene: RAPSN HGNC NCBI

Linked Data

ClinVar Variation Id: 2435363
ClinVar RCV Id: RCV003135204
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116034.2:p.Met233Val
CA5976662
NM_032645.5:c.697A>G