Canonical Allele Identifier: PA658672913
Gene: NGF HGNC NCBI

Linked Data

ClinVar Variation Id: 456625
ClinVar RCV Id: RCV000532480 RCV002384048
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002497.2:p.Asp45Asn
CA341837166
NM_002506.3:c.133G>A