Canonical Allele Identifier: PA2499269085
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1051675
ClinVar RCV Id: RCV001359745

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004792.1:p.Pro100Arg
CA346824278
NM_004801.6:c.299C>G