Canonical Allele Identifier: PA2827286937
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 206235
ClinVar RCV Id: RCV000188264 RCV003509510 RCV000765690 RCV002426909
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317011.1:p.Arg88Gly
CA316119
NM_001330082.2:c.262C>G