Canonical Allele Identifier: PA2827321195
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 852274
ClinVar RCV Id: RCV001056846
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317024.1:p.Asp931Glu
CA346776754
NM_001330095.2:c.2793T>G
CA346776755
NM_001330095.2:c.2793T>A