Canonical Allele Identifier: PA2827293517
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1354987
ClinVar RCV Id: RCV001866694
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317013.1:p.Gly927Arg
CA47360466
NM_001330084.2:c.2779G>A
CA346776753
NM_001330084.2:c.2779G>C