Canonical Allele Identifier: PA658805871
Gene: RAPSN HGNC NCBI

Linked Data

ClinVar Variation Id: 542733
ClinVar RCV Id: RCV000653215 RCV001835896
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005046.2:p.Arg337Cys
CA380327816
NM_005055.5:c.1009C>T