Canonical Allele Identifier: PA2827315779
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3024297
ClinVar RCV Id: RCV003883343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317023.1:p.Ala105Gly
CA346824252
NM_001330094.2:c.314C>G