Canonical Allele Identifier: PA2827317705
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 852274
ClinVar RCV Id: RCV001056846
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317023.1:p.Asp944Glu
CA346776754
NM_001330094.2:c.2832T>G
CA346776755
NM_001330094.2:c.2832T>A