Canonical Allele Identifier: PA2827294170
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1407592
ClinVar RCV Id: RCV001937829
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317013.1:p.Asn1222Ser
CA346820186
NM_001330084.2:c.3665A>G