Canonical Allele Identifier: PA916071625
Gene: RAPSN HGNC NCBI

Linked Data

ClinVar Variation Id: 8054
ClinVar RCV Id: RCV000008520 RCV000415079 RCV001343279 RCV003466839
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116034.2:p.Arg164Cys
CA119256
NM_032645.5:c.490C>T