Canonical Allele Identifier: PA2828181048
Gene: NLGN4Y HGNC NCBI

Linked Data

ClinVar Variation Id: 391879
ClinVar RCV Id: RCV000443711
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001352513.1:p.Asn421Lys
CA16609219
NM_001365584.1:c.1263C>A
CA415020285
NM_001365584.1:c.1263C>G