Canonical Allele Identifier: PA2573223436
Gene: NGF HGNC NCBI

Linked Data

ClinVar Variation Id: 1484755
ClinVar RCV Id: RCV002006037 RCV003312033
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002497.2:p.Ser138Gly
CA341836608
NM_002506.3:c.412A>G