Canonical Allele Identifier: PA2827306965
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 852274
ClinVar RCV Id: RCV001056846

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317017.1:p.Asp921Glu
CA346776754
NM_001330088.2:c.2763T>G
CA346776755
NM_001330088.2:c.2763T>A