Canonical Allele Identifier: PA2827285838
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 573853
ClinVar RCV Id: RCV000695626
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317007.1:p.Gly1259Arg
CA346820097
NM_001330078.2:c.3775G>C