Canonical Allele Identifier: PA2827308017
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 206231
ClinVar RCV Id: RCV000188260 RCV001060695
ClinVar Variation Id: 2016054
ClinVar RCV Id: RCV002843707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317018.1:p.Glu73Asp
CA316111
NM_001330089.2:c.219G>C
CA346824443
NM_001330089.2:c.219G>T