Canonical Allele Identifier: PA2741914467
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2818159
ClinVar RCV Id: RCV003620813

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004792.1:p.Phe93Leu
CA48054925
NM_004801.6:c.279C>G
CA346824321
NM_004801.6:c.279C>A
CA346824327
NM_004801.6:c.277T>C