Canonical Allele Identifier: PA2499269945
Gene: RAPSN HGNC NCBI

Linked Data

ClinVar Variation Id: 1016297
ClinVar RCV Id: RCV001315283
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005046.2:p.Gly284Arg
CA380329294
NM_005055.5:c.850G>C
CA380329296
NM_005055.5:c.850G>A