Canonical Allele Identifier: PA2827310222
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 573853
ClinVar RCV Id: RCV000695626
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317020.1:p.Gly224Arg
CA346820097
NM_001330091.2:c.670G>C