Canonical Allele Identifier: PA2580158207
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2072711
ClinVar RCV Id: RCV002967309

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129131.1:p.Ser330Phe
CA346822603
NM_001135659.2:c.989C>T