Canonical Allele Identifier: PA645429106
Gene: NRXN3 HGNC NCBI

Linked Data

ClinVar Variation Id: 375395
ClinVar RCV Id: RCV000416434

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004787.2:p.Lys66Glu
CA16044234
NM_004796.6:c.196A>G