Canonical Allele Identifier: PA2827305964
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 206257

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317017.1:p.Arg247Gly
CA316161
NM_001330088.2:c.739C>G