Canonical Allele Identifier: PA2573293038
Gene: RAPSN HGNC NCBI

Linked Data

ClinVar Variation Id: 1467269
ClinVar RCV Id: RCV001966289

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116034.2:p.Ala253Thr
CA380330101
NM_032645.5:c.757G>A