Allele Registry

Canonical Allele Identifier: PA106111

Gene: NGF HGNC NCBI

ClinVar RCV:

RCV000015089

RCV003989104

ClinVar Variation:

14045

HGVS (amino-acid)	Matching Registered Transcripts
NP_002497.2:p.Arg221Trp	CA123732 NM_002506.3:c.661C>T