Canonical Allele Identifier: PA2827284827
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 206227
ClinVar RCV Id: RCV000188256 RCV000764447 RCV000798181 RCV002317130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317007.1:p.Ala101Gly
CA316103
NM_001330078.2:c.302C>G