Canonical Allele Identifier: PA658672932
Gene: NGF HGNC NCBI

Linked Data

ClinVar Variation Id: 456629
ClinVar RCV Id: RCV000546440 RCV000603122
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002497.2:p.Val72Met
CA1023024
NM_002506.3:c.214G>A