Canonical Allele Identifier: PA645428336
Gene: NLGN4X HGNC NCBI

Linked Data

ClinVar Variation Id: 284715
ClinVar Variation Id: 2430488
ClinVar RCV Id: RCV003129047

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_851849.1:p.Arg753Ser
CA10604882
NM_181332.3:c.2259G>C
CA412012632
NM_181332.3:c.2259G>T