Canonical Allele Identifier: PA2827302329
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3012423
ClinVar RCV Id: RCV003875550

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317016.1:p.Asp106Ala
CA346824250
NM_001330087.2:c.317A>C