Canonical Allele Identifier: PA2829568608
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2072711
ClinVar RCV Id: RCV002967309

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004792.1:p.Ser297Phe
CA346822603
NM_004801.6:c.890C>T