Canonical Allele Identifier: PA2827309631
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 206257
ClinVar RCV Id: RCV000188288 RCV000792500 RCV001257611
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317019.1:p.Arg247Gly
CA316161
NM_001330090.2:c.739C>G