Canonical Allele Identifier: PA1139688778
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 852274
ClinVar RCV Id: RCV001056846

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129131.1:p.Asp988Glu
CA346776754
NM_001135659.2:c.2964T>G
CA346776755
NM_001135659.2:c.2964T>A