Canonical Allele Identifier: PA2829573558
Gene: RELN HGNC NCBI

Linked Data

ClinVar Variation Id: 2926467
ClinVar RCV Id: RCV003788705
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005036.2:p.Val2119Ala
CA4420968
NM_005045.4:c.6356T>C