Canonical Allele Identifier: PA2829573581
Gene: RELN HGNC NCBI

Linked Data

ClinVar Variation Id: 1025001
ClinVar RCV Id: RCV001325257
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005036.2:p.Pro2152Ser
CA368770971
NM_005045.4:c.6454C>T