Canonical Allele Identifier: PA204847
Gene: NTF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 208763
ClinVar RCV Id: RCV000190785
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006170.1:p.Gln174Arg
CA204846
NM_006179.5:c.521A>G