Canonical Allele Identifier: PA891848783
Gene: RELN HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005036.2:p.Asn587Ser
CA368765265
NM_005045.4:c.1760A>G