Canonical Allele Identifier: PA2499261827
Gene: NGF HGNC NCBI

Linked Data

ClinVar Variation Id: 1028026
ClinVar RCV Id: RCV001328962
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002497.2:p.Arg75Lys
CA1023021
NM_002506.3:c.224G>A