Allele Registry

Canonical Allele Identifier: PA645496198

Gene: NGF HGNC NCBI

ClinVar RCV:

RCV000268865

RCV001618498

RCV001699424

ClinVar Variation:

291993

HGVS (amino-acid)	Matching Registered Transcripts
NP_002497.2:p.Ala35Val	CA1023067 NM_002506.3:c.104C>T