Canonical Allele Identifier: PA154929
Gene: RELN HGNC NCBI

Linked Data

ClinVar Variation Id: 130133
ClinVar RCV Id: RCV000118162 RCV000290302 RCV000513733 RCV001082701 RCV001252608 RCV002490808
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005036.2:p.Gly2115Ser
CA154928
NM_005045.4:c.6343G>A