Canonical Allele Identifier: PA2827317708
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1354987
ClinVar RCV Id: RCV001866694
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317023.1:p.Gly945Arg
CA47360466
NM_001330094.2:c.2833G>A
CA346776753
NM_001330094.2:c.2833G>C