Canonical Allele Identifier: PA2827298713
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2818159
ClinVar RCV Id: RCV003620813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317015.1:p.Phe93Leu
CA48054925
NM_001330086.2:c.279C>G
CA346824321
NM_001330086.2:c.279C>A
CA346824327
NM_001330086.2:c.277T>C