Canonical Allele Identifier: PA2827298731
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1057573
ClinVar RCV Id: RCV001366586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317015.1:p.Glu99Ala
CA1655528
NM_001330086.2:c.296A>C