Canonical Allele Identifier: PA916064657
Gene: RELN HGNC NCBI

Linked Data

ClinVar Variation Id: 475951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_774959.1:p.Gln771His
CA4422015
NM_173054.3:c.2313G>T
CA368760451
NM_173054.3:c.2313G>C