Canonical Allele Identifier: PA2827305397
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2067777
ClinVar RCV Id: RCV002970642
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317017.1:p.Ile82Leu
CA346824388
NM_001330088.2:c.244A>C