Canonical Allele Identifier: PA658677501
Gene: RELN HGNC NCBI

Linked Data

ClinVar Variation Id: 475951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005036.2:p.Gln771His
CA4422015
NM_005045.4:c.2313G>T
CA368760451
NM_005045.4:c.2313G>C