Canonical Allele Identifier: PA658672922
Gene: NGF HGNC NCBI

Linked Data

ClinVar Variation Id: 456627
ClinVar RCV Id: RCV000553133 RCV004553172 RCV002413446
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002497.2:p.Ala58Val
CA1023046
NM_002506.3:c.173C>T