Canonical Allele Identifier: PA1139751837
Gene: RAPSN HGNC NCBI

Linked Data

ClinVar Variation Id: 970718

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116034.2:p.Arg257Trp
CA5976646
NM_032645.5:c.769C>T