Canonical Allele Identifier: PA2827286130
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3202225
ClinVar RCV Id: RCV004493637
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317008.1:p.Gly74Asp
CA346824439
NM_001330079.2:c.221G>A