Canonical Allele Identifier: PA2829576271
Gene: RAPSN HGNC NCBI

Linked Data

ClinVar Variation Id: 1495222
ClinVar RCV Id: RCV002028219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005046.2:p.Arg242Pro
CA5976655
NM_005055.5:c.725G>C