Canonical Allele Identifier: PA2499261825
Gene: NGF HGNC NCBI

Linked Data

ClinVar Variation Id: 1024609
ClinVar RCV Id: RCV001324816
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002497.2:p.Val63Met
CA1023038
NM_002506.3:c.187G>A