Canonical Allele Identifier: PA658832013
Gene: RAPSN HGNC NCBI

Linked Data

ClinVar Variation Id: 8046
ClinVar RCV Id: RCV000008512 RCV000170316 RCV000235028 RCV000224062 RCV000286918 RCV000414829 RCV000477955 RCV002512909 RCV003466838
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116034.2:p.Asn88Lys
CA199511
NM_032645.5:c.264C>A
CA380334837
NM_032645.5:c.264C>G