Canonical Allele Identifier: PA316162
Gene: NRXN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 206257
ClinVar RCV Id: RCV000188288 RCV000792500 RCV001257611
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001129131.1:p.Arg247Gly
CA316161
NM_001135659.2:c.739C>G