Allele Registry

Canonical Allele Identifier: PA099822

Gene: RAPSN HGNC NCBI

ClinVar RCV:

RCV000008524

ClinVar Variation:

8058

HGVS (amino-acid)	Matching Registered Transcripts
NP_005046.2:p.Phe139Ser	CA119259 NM_005055.5:c.416T>C