Canonical Allele Identifier: PA916065558
Gene: RELN HGNC NCBI

Linked Data

ClinVar Variation Id: 660465
ClinVar RCV Id: RCV000817661

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_774959.1:p.Pro3393Ser
CA4420038
NM_173054.3:c.10177C>T