Canonical Allele Identifier: PA2828181089
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_001352522.1:p.Asn401Lys
CA16609219
NM_001365593.1:c.1203C>A
CA415020285
NM_001365593.1:c.1203C>G