Canonical Allele Identifier: PA2829246841
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_001382418.1:p.Gln174Arg
CA204846
NM_001395489.1:c.521A>G