Canonical Allele Identifier: PA2825797913
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3202239
ClinVar RCV Id: RCV004493651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129131.1:p.His272Leu
CA346823198
NM_001135659.2:c.815A>T