Canonical Allele Identifier: PA2827293515
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 852274
ClinVar RCV Id: RCV001056846

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317013.1:p.Asp926Glu
CA346776754
NM_001330084.2:c.2778T>G
CA346776755
NM_001330084.2:c.2778T>A