Canonical Allele Identifier: PA915981097
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 206231
ClinVar Variation Id: 2016054
ClinVar RCV Id: RCV002843707

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004792.1:p.Glu73Asp
CA316111
NM_004801.6:c.219G>C
CA346824443
NM_004801.6:c.219G>T