Canonical Allele Identifier: PA658816826
Gene: NGF HGNC NCBI

Linked Data

ClinVar Variation Id: 526750
ClinVar RCV Id: RCV000631363 RCV002420680
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002497.2:p.Arg68Cys
CA1023028
NM_002506.3:c.202C>T