Canonical Allele Identifier: PA2829576253
Gene: RAPSN HGNC NCBI

Linked Data

ClinVar Variation Id: 2435363
ClinVar RCV Id: RCV003135204

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005046.2:p.Met233Val
CA5976662
NM_005055.5:c.697A>G