Canonical Allele Identifier: PA2827287739
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 852274
ClinVar RCV Id: RCV001056846

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317011.1:p.Asp940Glu
CA346776754
NM_001330082.2:c.2820T>G
CA346776755
NM_001330082.2:c.2820T>A