Allele Registry

Canonical Allele Identifier: PA123708

Gene: NTF4 HGNC NCBI

ClinVar Allele:

29057

ClinVar RCV:

RCV000015061

ClinVar Variation:

14018

HGVS (amino-acid)	Matching Registered Transcripts
NP_006170.1:p.Arg206Trp	CA123707 NM_006179.5:c.616C>T