Canonical Allele Identifier: PA2580277919
Gene: NGF HGNC NCBI
ClinVar RCV:
RCV003054394
ClinVar Variation:
2118913
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002497.2:p.Phe113Ser
CA341836773
NM_002506.3:c.338T>C