Canonical Allele Identifier: PA2827295238
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2999440
ClinVar RCV Id: RCV003852071

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317014.1:p.Asp106Gly
CA1655522
NM_001330085.2:c.317A>G