Canonical Allele Identifier: PA915981083
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 539881
ClinVar RCV Id: RCV000649739

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004792.1:p.Gly38Asp
CA346824686
NM_004801.6:c.113G>A