Canonical Allele Identifier: PA2827305534
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1315746
ClinVar RCV Id: RCV001755408

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317017.1:p.Asp106His
CA48054920
NM_001330088.2:c.316G>C