Canonical Allele Identifier: PA099778
Gene: RAPSN HGNC NCBI

Linked Data

ClinVar Variation Id: 8046
ClinVar RCV Id: RCV000008512 RCV000170316 RCV000235028 RCV000224062 RCV000286918 RCV000414829 RCV000477955 RCV002512909 RCV003466838
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005046.2:p.Asn88Lys
CA199511
NM_005055.5:c.264C>A
CA380334837
NM_005055.5:c.264C>G