Canonical Allele Identifier: PA2827309130
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 195130
ClinVar RCV Id: RCV001035816 RCV000656993 RCV000765689 RCV002252019 RCV002426841
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001317019.1:p.Gln90His
CA241414
NM_001330090.2:c.270G>T
CA346824342
NM_001330090.2:c.270G>C