Canonical Allele Identifier: PA2827270078
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_001316630.1:p.His238Tyr
CA174715
NM_001329701.2:c.712C>T