Canonical Allele Identifier: PA645392992
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_055708.3:p.Asn401Lys
CA16609219
NM_014893.5:c.1203C>A
CA415020285
NM_014893.5:c.1203C>G