Canonical Allele Identifier: PA174716
Gene: NTN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 161749
ClinVar RCV Id: RCV000149285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_067052.2:p.His275Tyr
CA174715
NM_021229.4:c.823C>T