Canonical Allele Identifier: PA2826601029
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_001269075.1:p.Arg753Ser
CA10604882
NM_001282146.2:c.2259G>C
CA412012632
NM_001282146.2:c.2259G>T